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Previous release (v1)
2024-05-19 10:29:23, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001319065 881 bp mRNA linear PRI 28-DEC-2022
DEFINITION Homo sapiens chorionic gonadotropin subunit beta 2 (CGB2),
transcript variant 2, mRNA.
ACCESSION NM_001319065 XM_005258480
VERSION NM_001319065.2
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 881)
AUTHORS Burczynska BB, Kobrouly L, Butler SA, Naase M and Iles RK.
TITLE Novel insights into the expression of CGB1 & 2 genes by epithelial
cancer cell lines secreting ectopic free hCGbeta
JOURNAL Anticancer Res 34 (5), 2239-2248 (2014)
PUBMED 24778026
REFERENCE 2 (bases 1 to 881)
AUTHORS Kubiczak M, Walkowiak GP, Nowak-Markwitz E and Jankowska A.
TITLE Human chorionic gonadotropin beta subunit genes CGB1 and CGB2 are
transcriptionally active in ovarian cancer
JOURNAL Int J Mol Sci 14 (6), 12650-12660 (2013)
PUBMED 23774837
REMARK GeneRIF: The presence of CGB1 and CGB2 transcripts in 41% of
analyzed ovarian cancer cases, is reported.
Publication Status: Online-Only
REFERENCE 3 (bases 1 to 881)
AUTHORS Goto-Kazeto R, Kazeto Y and Trant JM.
TITLE Molecular cloning, characterization and expression of
thyroid-stimulating hormone receptor in channel catfish
JOURNAL Gen Comp Endocrinol 161 (3), 313-319 (2009)
PUBMED 19523396
REFERENCE 4 (bases 1 to 881)
AUTHORS Rull K, Hallast P, Uuskula L, Jackson J, Punab M, Salumets A,
Campbell RK and Laan M.
TITLE Fine-scale quantification of HCG beta gene transcription in human
trophoblastic and non-malignant non-trophoblastic tissues
JOURNAL Mol Hum Reprod 14 (1), 23-31 (2008)
PUBMED 18048458
REFERENCE 5 (bases 1 to 881)
AUTHORS Hallast P, Rull K and Laan M.
TITLE The evolution and genomic landscape of CGB1 and CGB2 genes
JOURNAL Mol Cell Endocrinol 260-262 (9), 2-11 (2007)
PUBMED 17055150
REMARK GeneRIF: In silico prediction of putative transcription factor
binding sites supports the hypothesis that CGB1 and CGB2 gene
products are expressed in, and may contribute to, implantation and
placental development.
REFERENCE 6 (bases 1 to 881)
AUTHORS Bo M and Boime I.
TITLE Identification of the transcriptionally active genes of the
chorionic gonadotropin beta gene cluster in vivo
JOURNAL J Biol Chem 267 (5), 3179-3184 (1992)
PUBMED 1371113
REFERENCE 7 (bases 1 to 881)
AUTHORS Policastro,P.F., Daniels-McQueen,S., Carle,G. and Boime,I.
TITLE A map of the hCG beta-LH beta gene cluster
JOURNAL J Biol Chem 261 (13), 5907-5916 (1986)
PUBMED 2422163
REFERENCE 8 (bases 1 to 881)
AUTHORS Julier,C., Weil,D., Couillin,P., Cote,J.C., Nguyen,V.C.,
Foubert,C., Boue,A., Thirion,J.P., Kaplan,J.C. and Junien,C.
TITLE The beta chorionic gonadotropin-beta luteinizing gene cluster maps
to human chromosome 19
JOURNAL Hum Genet 67 (2), 174-177 (1984)
PUBMED 6204923
REFERENCE 9 (bases 1 to 881)
AUTHORS Policastro,P., Ovitt,C.E., Hoshina,M., Fukuoka,H., Boothby,M.R. and
Boime,I.
TITLE The beta subunit of human chorionic gonadotropin is encoded by
multiple genes
JOURNAL J Biol Chem 258 (19), 11492-11499 (1983)
PUBMED 6194155
REFERENCE 10 (bases 1 to 881)
AUTHORS Talmadge,K., Boorstein,W.R. and Fiddes,J.C.
TITLE The human genome contains seven genes for the beta-subunit of
chorionic gonadotropin but only one gene for the beta-subunit of
luteinizing hormone
JOURNAL DNA 2 (4), 281-289 (1983)
PUBMED 6319099
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AC008687.5.
On May 6, 2020 this sequence version replaced NM_001319065.1.
Summary: The beta subunit of chorionic gonadotropin (CGB) is
encoded by six highly homologous and structurally similar genes
that are arranged in tandem and inverted pairs on chromosome
19q13.3, and contiguous with the luteinizing hormone beta (LHB)
subunit gene. The CGB genes are primarily distinguished by
differences in the 5' untranscribed region. This gene was
originally thought to be one of the two pseudogenes (CGB1 and CGB2)
of CGB subunit, however, detection of CGB1 and CGB2 transcripts in
vivo, and their presence on the polysomes, suggested that these
transcripts are translated. To date, a protein product
corresponding to CGB2 has not been isolated. The deduced sequence
of the hypothetical protein of 132 aa does not share any similarity
with that of functional CGB subunits (PMID:8954017). However, a 163
aa protein, translated from a different frame, is about the same
size, and shares 98% identity with other CGB subunits. [provided by
RefSeq, Jul 2008].
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: BC107143.1, GE745565.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA2145893, SAMEA2150585
[ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-381 AC008687.5 43198-43578
382-549 AC008687.5 43812-43979
550-881 AC008687.5 44215-44546
FEATURES Location/Qualifiers
source 1..881
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19q13.33"
gene 1..881
/gene="CGB2"
/note="chorionic gonadotropin subunit beta 2"
/db_xref="GeneID:114336"
/db_xref="HGNC:HGNC:16722"
/db_xref="MIM:608824"
exon 1..381
/gene="CGB2"
/inference="alignment:Splign:2.1.0"
variation 2
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:148507179"
variation 3
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1252312324"
variation 6
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039737254"
variation 7
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413032839"
variation 8
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1200906270"
variation 9
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1051611638"
variation 10
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600218789"
variation 12
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407251673"
variation 13
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:945343533"
variation 15
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319062595"
variation 16
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1041617148"
variation 17..20
/gene="CGB2"
/replace="cgcc"
/replace="cgccgcc"
/db_xref="dbSNP:1331870499"
variation 17
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1227501415"
variation 18
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039737629"
variation 19..23
/gene="CGB2"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1397779621"
variation 19
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:370625414"
variation 20
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342397130"
variation 21
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1220554114"
variation 22
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1000447906"
variation 23
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:111778275"
variation 25
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1263395025"
variation 26
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:539621609"
variation 27
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1012709065"
variation 28..30
/gene="CGB2"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:894283393"
variation 28
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039737899"
variation 29
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600218841"
variation 30
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122129918"
variation 32
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039738000"
variation 33
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039738042"
variation 35..40
/gene="CGB2"
/replace="agggga"
/replace="aggggagggga"
/db_xref="dbSNP:2039738123"
variation 35
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1206591460"
variation 37
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:878910891"
variation 39
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039738179"
variation 40
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039738208"
variation 41
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:558470323"
variation 42
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1317528525"
variation 44
/gene="CGB2"
/replace=""
/replace="g"
/db_xref="dbSNP:1249806863"
variation 44
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1309905175"
variation 45
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:113072693"
variation 46
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1374433739"
variation 47
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330396053"
variation 49
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039738388"
variation 50..58
/gene="CGB2"
/replace="gagagag"
/replace="gagagagag"
/replace="gagagagagag"
/db_xref="dbSNP:971061169"
variation 51
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1300646033"
variation 58
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:373835095"
variation 60
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1015872671"
variation 61
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1477101101"
variation 62
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:562367130"
variation 64
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039738611"
variation 65
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1178795535"
variation 66
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:962964697"
variation 67..77
/gene="CGB2"
/replace="tgggtccgctg"
/replace="tgggtccgctgggtccgctg"
/db_xref="dbSNP:2039738723"
variation 67
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039738691"
variation 68
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:575459119"
variation 69
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039738812"
variation 70
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1254346655"
variation 72
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1456983605"
variation 73
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1028529819"
variation 74
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600218917"
variation 76
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1351395479"
variation 78
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039739081"
variation 81
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1157478904"
variation 82
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:190529587"
variation 83
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:375800569"
variation 84
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395049383"
variation 85
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:986910746"
variation 86
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1418473251"
variation 87
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:141047975"
variation 88
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473987610"
variation 92..105
/gene="CGB2"
/replace="cccgtgccgcgtcc"
/replace="cccgtgccgcgtccccgtgccgcgtcc"
/db_xref="dbSNP:1047171305"
variation 92
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039739439"
variation 94
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371513652"
variation 95
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1283447391"
variation 97
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328128310"
variation 98
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2122130316"
variation 99
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039739633"
variation 100
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1487963552"
variation 101
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:925276326"
variation 102
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358241821"
variation 104
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039739769"
variation 107
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1226336595"
variation 108
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039739826"
variation 110
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1269844801"
variation 111
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351276056"
variation 112
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:935959576"
variation 113
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600218992"
variation 114
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2122130406"
variation 115
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039740078"
variation 116
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397595812"
variation 117
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209126999"
variation 120
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568656445"
variation 121..122
/gene="CGB2"
/replace=""
/replace="ct"
/db_xref="dbSNP:2039740192"
variation 122
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039740221"
variation 123
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039740251"
variation 126
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039740284"
variation 129
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:777197144"
variation 130
/gene="CGB2"
/replace=""
/replace="t"
/db_xref="dbSNP:1324810632"
variation 130
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449879940"
variation 131..135
/gene="CGB2"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:2039740433"
variation 131
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407540858"
variation 132
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054780067"
variation 133
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:374187968"
variation 134
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749218851"
variation 135
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:560269918"
variation 136
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199541035"
variation 137
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1472415190"
variation 139
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600219066"
variation 141
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:144946613"
variation 143
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:147920450"
variation 145
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039740769"
variation 146
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039740798"
variation 150
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1318251457"
variation 153
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2122130612"
variation 154
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122130618"
variation 155
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039740829"
variation 156
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:759752792"
variation 158
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1460993645"
variation 159
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1182757115"
variation 160
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1338220244"
variation 161
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039740988"
variation 163
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039741019"
variation 164
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039741048"
variation 166
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:564264943"
variation 168..171
/gene="CGB2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1439289148"
variation 168
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373500607"
variation 170
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:756253760"
variation 171
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:778235622"
variation 174
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:754390557"
variation 175
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:757586036"
variation 178
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:779207058"
variation 179
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:778838356"
variation 180
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039741350"
variation 181
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746243374"
variation 185
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:376112335"
variation 189
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568656517"
variation 190
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039741500"
variation 191
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200144335"
variation 192
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1383097675"
variation 193
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746524605"
variation 194
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1325146902"
variation 196..199
/gene="CGB2"
/replace=""
/replace="aaga"
/db_xref="dbSNP:2039741719"
variation 196
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:768343718"
variation 197..205
/gene="CGB2"
/replace="agagaga"
/replace="agagagaga"
/db_xref="dbSNP:766849487"
variation 197
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1426020073"
variation 198
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:201932007"
variation 199..225
/gene="CGB2"
/replace="aga"
/replace="agagagacatgtcaaaggtagggtaga"
/db_xref="dbSNP:1174379119"
variation 199
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1235528617"
variation 200
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:745603008"
variation 201
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1367190127"
variation 202
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1322906998"
variation 204..206
/gene="CGB2"
/replace=""
/replace="gac"
/db_xref="dbSNP:1463998004"
variation 204
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202070796"
variation 207
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776690641"
variation 208
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769885964"
variation 209
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1205456854"
variation 211
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:772999884"
variation 212
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:762657356"
variation 213
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:767771534"
variation 214
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039742291"
variation 215
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:529234095"
variation 216
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:760721079"
variation 217
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039742394"
variation 218
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:764198325"
variation 219
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:753948430"
variation 220..224
/gene="CGB2"
/replace="ggtag"
/replace="ggtaggtag"
/db_xref="dbSNP:1220452724"
variation 220
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375347097"
variation 221
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765677461"
variation 223
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:201307885"
variation 224
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1383441948"
variation 225
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201727056"
variation 227
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:370856581"
variation 228
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:35414741"
variation 231
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374802163"
variation 232
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039742881"
variation 234
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:112416411"
variation 235
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039742937"
variation 236
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:747672721"
variation 237
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:769785547"
variation 238
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:749092663"
variation 239
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1260002513"
variation 240
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:770680961"
variation 242
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:775750042"
variation 243
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760845814"
variation 244
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1490053178"
variation 245
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367740459"
variation 247
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039743239"
variation 248
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1409722789"
variation 250
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200232165"
variation 251
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568656594"
variation 254
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:376136197"
variation 255
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1362476020"
variation 256
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:765770876"
variation 257
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1469373704"
variation 258
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:750951101"
variation 261
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:758772094"
variation 262
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039743566"
variation 263
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:752006539"
variation 264..266
/gene="CGB2"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1237706851"
variation 264
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:754630968"
variation 266
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:780994360"
variation 267
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:747654181"
variation 269
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039743741"
variation 271
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:990092630"
variation 273
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039743790"
variation 274
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039743840"
variation 275
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1278950436"
variation 276
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039743900"
variation 280
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218049125"
variation 281
/gene="CGB2"
/replace=""
/replace="t"
/db_xref="dbSNP:2039743958"
variation 282..284
/gene="CGB2"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1356448880"
variation 283
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:915776017"
variation 284
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187360503"
variation 285
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039744087"
variation 286
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039744109"
variation 288
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380277569"
variation 290
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039744166"
variation 291
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286198290"
variation 293
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039744224"
variation 294
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:767823358"
variation 297
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:143465240"
variation 298
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1045561954"
variation 306
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039744364"
variation 307
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:907022525"
variation 308
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039744434"
variation 309
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039744467"
variation 311
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039744488"
variation 316
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600219320"
variation 317
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1420297033"
variation 318
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1362377839"
variation 319
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1156766268"
variation 324
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:113992714"
variation 325
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039744667"
variation 327
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1369363280"
variation 328
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039744779"
variation 330
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2122131512"
variation 331
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471592060"
variation 332
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039744840"
variation 334
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:183740354"
variation 336
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:570203506"
variation 342
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039744952"
variation 344
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1600219349"
variation 345
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:10413257"
variation 346
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039745094"
variation 347
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:556013248"
variation 349
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039745153"
variation 351
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141087007"
variation 353
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:541845960"
variation 355
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1028590493"
variation 356
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1310387323"
variation 357
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:553946679"
variation 362
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1246572252"
variation 364
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039745400"
variation 365
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039745462"
variation 366
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1008419223"
variation 370
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1296810771"
variation 371
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039745590"
variation 372
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:760347520"
misc_feature 373..375
/gene="CGB2"
/note="upstream in-frame stop codon"
variation 374
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039745674"
variation 376..380
/gene="CGB2"
/replace="ccc"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:2039745702"
variation 377
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:111811197"
variation 378
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203112737"
variation 379
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:545834903"
exon 382..549
/gene="CGB2"
/inference="alignment:Splign:2.1.0"
variation 382
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144929524"
variation 384
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275000963"
variation 385
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:752442097"
variation 387
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039751014"
variation 388
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755618431"
variation 391
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039751108"
variation 393
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1203158627"
variation 394
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039751188"
variation 396
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039751223"
variation 397
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1258023501"
variation 398
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039751308"
variation 399
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039751351"
variation 405..407
/gene="CGB2"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:754154187"
variation 408
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:777107163"
CDS 409..864
/gene="CGB2"
/note="isoform 2 is encoded by transcript variant 2;
product of CGB2; chorionic gonadotropin beta subunit 2;
chorionic gonadotropin, beta polypeptide 2"
/codon_start=1
/product="choriogonadotropin subunit beta variant 2
isoform 2"
/protein_id="NP_001305994.1"
/db_xref="GeneID:114336"
/db_xref="HGNC:HGNC:16722"
/db_xref="MIM:608824"
/translation="
MGGTWASKEPLRPRCRPINATLAVEKEGCPVCITVNTTICAGYCPTMTRVLQGVLPALPQVVCNYRDVRFESIRLPGCPRGVNPVVSYAVALSCQCALCRRSTTDCGGPKDHPLTCDDPRFQASSSSKAPPPSLPSPSRLPGPSDTPILPQ"
misc_feature 439..759
/gene="CGB2"
/note="Glycoprotein hormone beta chain homologues; Region:
GHB; smart00068"
/db_xref="CDD:214502"
misc_feature order(451..453,526..528,538..540,595..597,688..690,
694..696)
/gene="CGB2"
/note="cysteine knot motif; other site"
/db_xref="CDD:200450"
misc_feature order(472..474,481..483,523..564,592..597,703..705,
709..711,718..735)
/gene="CGB2"
/note="dimer interface [polypeptide binding]; other site"
/db_xref="CDD:200450"
misc_feature order(562..564,709..714,721..723,727..735)
/gene="CGB2"
/note="receptor binding site [polypeptide binding]; other
site"
/db_xref="CDD:200450"
variation 414
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1363196204"
variation 415
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753409584"
variation 416
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1443141509"
variation 417
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039751637"
variation 418
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200580991"
variation 419
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164019909"
variation 421
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600219796"
variation 422..424
/gene="CGB2"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:755362324"
variation 422
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:778828392"
variation 423
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039751900"
variation 424
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:745659081"
variation 425
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:771913092"
variation 426
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:931076371"
variation 427
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781369789"
variation 429
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:770090626"
variation 431
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:773120078"
variation 432
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1261222777"
variation 433
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1405140496"
variation 435
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:763110483"
variation 436
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:557817297"
variation 437
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576183783"
variation 438
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201386805"
variation 440
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1292908860"
variation 442
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:759953706"
variation 443
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:768029210"
variation 445
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039752690"
variation 446
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272451773"
variation 447
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262093314"
variation 448
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:753143101"
variation 449
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:543600196"
variation 450
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039752935"
variation 452
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1243216240"
variation 454
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369311910"
variation 455
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:58969991"
variation 456
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386588308"
variation 459
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039753233"
variation 463
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039753278"
variation 464
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:778810194"
variation 465
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:750411035"
variation 469
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039753408"
variation 470
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200322633"
variation 472
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122133303"
variation 478
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039753501"
variation 479
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368585502"
variation 480
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1297554465"
variation 481
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1427410257"
variation 482..486
/gene="CGB2"
/replace="ag"
/replace="agaag"
/db_xref="dbSNP:2039753677"
variation 483
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1412566642"
variation 486
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:746845618"
variation 487
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1345562185"
variation 489
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:769852318"
variation 494
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1296245349"
variation 495
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1166094103"
variation 498
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200622579"
variation 499
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749311600"
variation 500
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282271061"
variation 504
/gene="CGB2"
/replace=""
/replace="c"
/db_xref="dbSNP:1301742152"
variation 506
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049493124"
variation 510
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320906719"
variation 511
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:774963725"
variation 514
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:760080204"
variation 522
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1275640347"
variation 523
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039754394"
variation 525
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1194577707"
variation 527
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446769441"
variation 530
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339370300"
variation 531
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1214335268"
variation 537
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039754604"
variation 540
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1271638926"
variation 541..542
/gene="CGB2"
/replace=""
/replace="tt"
/db_xref="dbSNP:1490543220"
variation 542
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198723220"
variation 543
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427476410"
variation 545
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1471242055"
exon 550..881
/gene="CGB2"
/inference="alignment:Splign:2.1.0"
variation 550
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039758580"
variation 551
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039758620"
variation 552
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039758658"
variation 553
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1334015067"
variation 554
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1003520882"
variation 555
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039758861"
variation 556
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039758912"
variation 561
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039758955"
variation 562
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1425299265"
variation 563
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157557215"
variation 564..568
/gene="CGB2"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1568657286"
variation 564
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039759071"
variation 565
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039759153"
variation 566
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1162834291"
variation 567
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1388007458"
variation 568
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1411119142"
variation 569
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600220262"
variation 570
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1329160940"
variation 575
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395547400"
variation 576
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1035619346"
variation 577
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:961311976"
variation 578..580
/gene="CGB2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1171737664"
variation 579
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1334755644"
variation 580
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039759669"
variation 581
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039759710"
variation 582
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445044099"
variation 584
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430873896"
variation 587
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1416754920"
variation 588
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039759861"
variation 592
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1185477707"
variation 596
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:972655883"
variation 597
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254523668"
variation 598
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1211534519"
variation 599
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:567810797"
variation 603
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1383981126"
variation 604
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1245951914"
variation 606
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766320454"
variation 607
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1341598546"
variation 613
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1196406402"
variation 614
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272583296"
variation 616
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:535359388"
variation 618
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1185654733"
variation 619
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754856583"
variation 629
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039760503"
variation 631
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039760563"
variation 639
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:952570451"
variation 642
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777832687"
variation 644
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1182951421"
variation 646
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:749561224"
variation 647
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1476121050"
variation 648
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:985624945"
variation 649
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1395325750"
variation 650
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039760938"
variation 651
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039760983"
variation 652
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1463794919"
variation 653
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1338269947"
variation 654
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1407352731"
variation 655
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1452323632"
variation 657
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039761194"
variation 658
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039761231"
variation 659
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:368406891"
variation 660
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:565712351"
variation 661
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:539396284"
variation 663
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1269747914"
variation 664
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1247645780"
variation 665
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:943727292"
variation 669
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316133681"
variation 672
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039761572"
variation 673
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488389043"
variation 675
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:772638632"
variation 676
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1205864334"
variation 677
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:557614882"
variation 680
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:747322839"
variation 681
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039761851"
variation 683
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348692486"
variation 684
/gene="CGB2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2039761954"
variation 684
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282645205"
variation 688
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232352006"
variation 689
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199611687"
variation 691
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254010744"
variation 692
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448594994"
variation 693
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1193803729"
variation 694
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039762152"
variation 697
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:576078244"
variation 699
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1476537923"
variation 700
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776116585"
variation 702
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1298113670"
variation 706
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429495580"
variation 707
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469624203"
variation 709
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761415657"
variation 710
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039762547"
variation 713
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:536701296"
variation 716
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039762646"
variation 717
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376733996"
variation 719
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:772655900"
variation 724
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318219779"
variation 725
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433684763"
variation 726
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1299690131"
variation 727..731
/gene="CGB2"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:777455689"
variation 727
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:935606172"
variation 729
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039763054"
variation 731
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:762457255"
variation 732
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1284186901"
variation 733
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:766287907"
variation 735
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1232266016"
variation 737
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254093578"
variation 738
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039763324"
variation 740..745
/gene="CGB2"
/replace="acc"
/replace="accacc"
/db_xref="dbSNP:2039763367"
variation 741
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039763398"
variation 742
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:879087230"
variation 744..747
/gene="CGB2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:751185623"
variation 745
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039763515"
variation 746
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751562126"
variation 750
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262341834"
variation 753
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2122135428"
variation 754
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259676447"
variation 755
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1487035340"
variation 757
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:767299343"
variation 759
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269164577"
variation 761
/gene="CGB2"
/replace=""
/replace="a"
/db_xref="dbSNP:2039763828"
variation 762..766
/gene="CGB2"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1347373456"
variation 762
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:752456770"
variation 763
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:757496259"
variation 764
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:373937262"
variation 765
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039764062"
variation 766
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758610268"
variation 767
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:747591676"
variation 767
/gene="CGB2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:756866476"
variation 768
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1308626310"
variation 774
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039764295"
variation 775
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039764331"
variation 776
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:62126039"
variation 777
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:777010041"
variation 778
/gene="CGB2"
/replace=""
/replace="t"
/db_xref="dbSNP:1568657568"
variation 779
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:748530277"
variation 781
/gene="CGB2"
/replace=""
/replace="t"
/db_xref="dbSNP:2039764604"
variation 781
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:769372072"
variation 784
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:377550014"
variation 788
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:573468238"
variation 789
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318537464"
variation 790
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1321674757"
variation 793
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770511936"
variation 794
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759465267"
variation 795
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:371049621"
variation 796
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1224627287"
variation 797
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:760611871"
variation 798
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362997198"
variation 799..804
/gene="CGB2"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:780705864"
variation 799
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:540962781"
variation 800
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:750724523"
variation 801
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252175982"
variation 802
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122135778"
variation 803
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758523378"
variation 804
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200008626"
variation 807
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751614145"
variation 811
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:200930560"
variation 812
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1234321908"
variation 813..814
/gene="CGB2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:745327270"
variation 813
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039765588"
variation 814
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039765670"
variation 815
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781558432"
variation 816..818
/gene="CGB2"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1568657648"
variation 816
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059305"
variation 818
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039765868"
variation 820
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412918115"
variation 821
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:770189990"
variation 822
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039765997"
variation 823
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202133130"
variation 824
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770509172"
variation 825
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773852875"
variation 826
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:758972659"
variation 828
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772040659"
variation 829
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374370941"
variation 830
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248147513"
variation 831
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775624646"
variation 835
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:563497383"
variation 837
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:753717837"
variation 839
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:763186401"
variation 840
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:766526327"
variation 842..845
/gene="CGB2"
/replace="acac"
/replace="acacac"
/db_xref="dbSNP:769624942"
variation 842
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1600220838"
variation 843
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:531035587"
variation 845..848
/gene="CGB2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:775720135"
variation 845
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1014954743"
variation 846
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751595129"
variation 847
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1373697554"
variation 848
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413645086"
variation 849
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755083053"
variation 852
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172541024"
variation 853
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039767177"
variation 854
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600220876"
variation 856
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1470111522"
variation 857
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355182438"
variation 858
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781657887"
variation 859
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039767354"
regulatory 860..865
/regulatory_class="polyA_signal_sequence"
/gene="CGB2"
/note="hexamer: AATAAA"
variation 860
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329538280"
variation 861
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:549468046"
variation 862
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1454338129"
variation 863
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450244941"
variation 866
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756642481"
variation 868
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:994527785"
variation 871
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226118495"
variation 873..880
/gene="CGB2"
/replace=""
/replace="caatccgc"
/db_xref="dbSNP:1209752653"
variation 873
/gene="CGB2"
/replace=""
/replace="c"
/db_xref="dbSNP:749096000"
variation 873
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568657731"
variation 874..875
/gene="CGB2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1568657738"
variation 874
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1307550978"
variation 875
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:778059636"
variation 877..878
/gene="CGB2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:543759521"
variation 877
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:952657324"
variation 878
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374106963"
variation 879
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770548953"
variation 880
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:778495999"
polyA_site 881
/gene="CGB2"
/note="major polyA site"
variation 881
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:745368260"
ORIGIN
gccctgcgttccgtggcgccccctggagggaggaaggggaactgtatctgagagagagcagccaattgggtccgctgactccggccgggttcccgtgccgcgtccaacacccctcactccctgtctcactcccccacggagactcaatttactttccatgtccacatccccagtgcttgcggaagatatcccgctaagagagagacatgtcaaaggtagggtagatcgacatttccaggcaccaaagatggagatgttccaggaaagactgcagggcccctgggcaccttccacctgcttccaggccatcactggcatgagaaggggcagaccagtgtgagctgtggaaggaggcctctttctggaggagcgtgacccccagggctgctgctgttgctgctgctgagcatgggcgggacatgggcatccaaggagccgcttcggccacggtgccgccccatcaatgccaccctggctgtggagaaggagggctgccccgtgtgcatcaccgtcaacaccaccatctgtgccggctactgccccaccatgacccgcgtgctgcagggggtcctgccggccctgcctcaggtggtgtgcaactaccgcgatgtgcgcttcgagtccatccggctccctggctgcccgcgcggcgtgaaccccgtggtctcctacgccgtggctctcagctgtcaatgtgcactctgccgccgcagcaccactgactgcgggggtcccaaggaccaccccttgacctgtgatgacccccgcttccaggcctcctcttcctcaaaggcccctccccccagccttccaagcccatcccgactcccggggccctcagacaccccgatcctcccacaataaaggcttctcaatccgca
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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