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Previous release (v1)
2024-05-19 10:43:14, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_033378 715 bp mRNA linear PRI 29-DEC-2022
DEFINITION Homo sapiens chorionic gonadotropin subunit beta 2 (CGB2),
transcript variant 1, mRNA.
ACCESSION NM_033378
VERSION NM_033378.2
KEYWORDS RefSeq; MANE Select.
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 715)
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 715)
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 715)
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 715)
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 715)
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 715)
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 715)
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 715)
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 715)
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 715)
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_033378.1.
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 :: BC069367.1, AA393716.1 [ECO:0000332]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000359342.7/ ENSP00000352295.6
RefSeq Select criteria :: based on manual assertion, conservation,
expression, longest protein
##RefSeq-Attributes-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-215 AC008687.5 43198-43412
216-383 AC008687.5 43812-43979
384-715 AC008687.5 44215-44546
FEATURES Location/Qualifiers
source 1..715
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19q13.33"
gene 1..715
/gene="CGB2"
/note="chorionic gonadotropin subunit beta 2"
/db_xref="GeneID:114336"
/db_xref="HGNC:HGNC:16722"
/db_xref="MIM:608824"
exon 1..215
/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"
misc_feature 195..197
/gene="CGB2"
/note="upstream in-frame stop codon"
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
/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"
CDS 207..698
/gene="CGB2"
/note="isoform 1 precursor is encoded by transcript
variant 1; product of CGB2; chorionic gonadotropin beta
subunit 2; chorionic gonadotropin, beta polypeptide 2"
/codon_start=1
/product="choriogonadotropin subunit beta variant 2
isoform 1 precursor"
/protein_id="NP_203696.2"
/db_xref="CCDS:CCDS12750.2"
/db_xref="GeneID:114336"
/db_xref="HGNC:HGNC:16722"
/db_xref="MIM:608824"
/translation="
MSKGLLLLLLLSMGGTWASKEPLRPRCRPINATLAVEKEGCPVCITVNTTICAGYCPTMTRVLQGVLPALPQVVCNYRDVRFESIRLPGCPRGVNPVVSYAVALSCQCALCRRSTTDCGGPKDHPLTCDDPRFQASSSSKAPPPSLPSPSRLPGPSDTPILPQ"
sig_peptide 207..260
/gene="CGB2"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
mat_peptide 261..695
/gene="CGB2"
/product="Choriogonadotropin subunit beta variant 2.
/evidence=ECO:0000255. /id=PRO_0000342549"
/note="propagated from UniProtKB/Swiss-Prot (Q6NT52.5)"
misc_feature 273..593
/gene="CGB2"
/note="Glycoprotein hormone beta chain homologues; Region:
GHB; smart00068"
/db_xref="CDD:214502"
misc_feature order(285..287,360..362,372..374,429..431,522..524,
528..530)
/gene="CGB2"
/note="cysteine knot motif; other site"
/db_xref="CDD:200450"
misc_feature 297..299
/gene="CGB2"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q6NT52.5); glycosylation site"
misc_feature order(306..308,315..317,357..398,426..431,537..539,
543..545,552..569)
/gene="CGB2"
/note="dimer interface [polypeptide binding]; other site"
/db_xref="CDD:200450"
misc_feature 348..350
/gene="CGB2"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q6NT52.5); glycosylation site"
misc_feature order(396..398,543..548,555..557,561..569)
/gene="CGB2"
/note="receptor binding site [polypeptide binding]; other
site"
/db_xref="CDD:200450"
misc_feature 591..695
/gene="CGB2"
/note="propagated from UniProtKB/Swiss-Prot (Q6NT52.5);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
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"
exon 216..383
/gene="CGB2"
/inference="alignment:Splign:2.1.0"
variation 216
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144929524"
variation 218
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275000963"
variation 219
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:752442097"
variation 221
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039751014"
variation 222
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:755618431"
variation 225
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039751108"
variation 227
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1203158627"
variation 228
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039751188"
variation 230
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039751223"
variation 231
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1258023501"
variation 232
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039751308"
variation 233
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039751351"
variation 239..241
/gene="CGB2"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:754154187"
variation 242
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:777107163"
variation 248
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1363196204"
variation 249
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753409584"
variation 250
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1443141509"
variation 251
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039751637"
variation 252
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200580991"
variation 253
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164019909"
variation 255
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600219796"
variation 256..258
/gene="CGB2"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:755362324"
variation 256
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:778828392"
variation 257
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039751900"
variation 258
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:745659081"
variation 259
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:771913092"
variation 260
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:931076371"
variation 261
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781369789"
variation 263
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:770090626"
variation 265
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:773120078"
variation 266
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1261222777"
variation 267
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1405140496"
variation 269
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:763110483"
variation 270
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:557817297"
variation 271
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576183783"
variation 272
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201386805"
variation 274
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1292908860"
variation 276
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:759953706"
variation 277
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:768029210"
variation 279
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039752690"
variation 280
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272451773"
variation 281
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262093314"
variation 282
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:753143101"
variation 283
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:543600196"
variation 284
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039752935"
variation 286
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1243216240"
variation 288
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369311910"
variation 289
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:58969991"
variation 290
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386588308"
variation 293
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039753233"
variation 297
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039753278"
variation 298
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:778810194"
variation 299
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:750411035"
variation 303
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039753408"
variation 304
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200322633"
variation 306
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122133303"
variation 312
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039753501"
variation 313
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368585502"
variation 314
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1297554465"
variation 315
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1427410257"
variation 316..320
/gene="CGB2"
/replace="ag"
/replace="agaag"
/db_xref="dbSNP:2039753677"
variation 317
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1412566642"
variation 320
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:746845618"
variation 321
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1345562185"
variation 323
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:769852318"
variation 328
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1296245349"
variation 329
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1166094103"
variation 332
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200622579"
variation 333
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749311600"
variation 334
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282271061"
variation 338
/gene="CGB2"
/replace=""
/replace="c"
/db_xref="dbSNP:1301742152"
variation 340
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049493124"
variation 344
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320906719"
variation 345
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:774963725"
variation 348
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:760080204"
variation 356
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1275640347"
variation 357
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039754394"
variation 359
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1194577707"
variation 361
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446769441"
variation 364
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339370300"
variation 365
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1214335268"
variation 371
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039754604"
variation 374
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1271638926"
variation 375..376
/gene="CGB2"
/replace=""
/replace="tt"
/db_xref="dbSNP:1490543220"
variation 376
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198723220"
variation 377
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427476410"
variation 379
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1471242055"
exon 384..715
/gene="CGB2"
/inference="alignment:Splign:2.1.0"
variation 384
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039758580"
variation 385
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039758620"
variation 386
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039758658"
variation 387
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1334015067"
variation 388
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1003520882"
variation 389
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039758861"
variation 390
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039758912"
variation 395
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039758955"
variation 396
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1425299265"
variation 397
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157557215"
variation 398..402
/gene="CGB2"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1568657286"
variation 398
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039759071"
variation 399
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039759153"
variation 400
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1162834291"
variation 401
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1388007458"
variation 402
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1411119142"
variation 403
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600220262"
variation 404
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1329160940"
variation 409
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395547400"
variation 410
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1035619346"
variation 411
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:961311976"
variation 412..414
/gene="CGB2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1171737664"
variation 413
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1334755644"
variation 414
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039759669"
variation 415
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039759710"
variation 416
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445044099"
variation 418
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430873896"
variation 421
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1416754920"
variation 422
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039759861"
variation 426
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1185477707"
variation 430
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:972655883"
variation 431
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254523668"
variation 432
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1211534519"
variation 433
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:567810797"
variation 437
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1383981126"
variation 438
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1245951914"
variation 440
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:766320454"
variation 441
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1341598546"
variation 447
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1196406402"
variation 448
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272583296"
variation 450
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:535359388"
variation 452
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1185654733"
variation 453
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754856583"
variation 463
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039760503"
variation 465
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039760563"
variation 473
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:952570451"
variation 476
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777832687"
variation 478
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1182951421"
variation 480
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:749561224"
variation 481
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1476121050"
variation 482
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:985624945"
variation 483
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1395325750"
variation 484
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039760938"
variation 485
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039760983"
variation 486
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1463794919"
variation 487
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1338269947"
variation 488
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1407352731"
variation 489
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1452323632"
variation 491
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039761194"
variation 492
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039761231"
variation 493
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:368406891"
variation 494
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:565712351"
variation 495
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:539396284"
variation 497
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1269747914"
variation 498
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1247645780"
variation 499
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:943727292"
variation 503
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316133681"
variation 506
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039761572"
variation 507
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488389043"
variation 509
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:772638632"
variation 510
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1205864334"
variation 511
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:557614882"
variation 514
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:747322839"
variation 515
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039761851"
variation 517
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348692486"
variation 518
/gene="CGB2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2039761954"
variation 518
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282645205"
variation 522
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232352006"
variation 523
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199611687"
variation 525
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1254010744"
variation 526
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448594994"
variation 527
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1193803729"
variation 528
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039762152"
variation 531
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:576078244"
variation 533
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1476537923"
variation 534
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:776116585"
variation 536
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1298113670"
variation 540
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429495580"
variation 541
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469624203"
variation 543
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761415657"
variation 544
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039762547"
variation 547
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:536701296"
variation 550
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039762646"
variation 551
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376733996"
variation 553
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:772655900"
variation 558
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318219779"
variation 559
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433684763"
variation 560
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1299690131"
variation 561..565
/gene="CGB2"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:777455689"
variation 561
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:935606172"
variation 563
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039763054"
variation 565
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:762457255"
variation 566
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:1284186901"
variation 567
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:766287907"
variation 569
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1232266016"
variation 571
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254093578"
variation 572
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039763324"
variation 574..579
/gene="CGB2"
/replace="acc"
/replace="accacc"
/db_xref="dbSNP:2039763367"
variation 575
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039763398"
variation 576
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:879087230"
variation 578..581
/gene="CGB2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:751185623"
variation 579
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039763515"
variation 580
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751562126"
variation 584
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262341834"
variation 587
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:2122135428"
variation 588
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259676447"
variation 589
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1487035340"
variation 591
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:767299343"
variation 593
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269164577"
variation 595
/gene="CGB2"
/replace=""
/replace="a"
/db_xref="dbSNP:2039763828"
variation 596..600
/gene="CGB2"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1347373456"
variation 596
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:752456770"
variation 597
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:757496259"
variation 598
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:373937262"
variation 599
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039764062"
variation 600
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758610268"
variation 601
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:747591676"
variation 601
/gene="CGB2"
/replace="g"
/replace="gg"
/db_xref="dbSNP:756866476"
variation 602
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1308626310"
variation 608
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039764295"
variation 609
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039764331"
variation 610
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:62126039"
variation 611
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:777010041"
variation 612
/gene="CGB2"
/replace=""
/replace="t"
/db_xref="dbSNP:1568657568"
variation 613
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:748530277"
variation 615
/gene="CGB2"
/replace=""
/replace="t"
/db_xref="dbSNP:2039764604"
variation 615
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:769372072"
variation 618
/gene="CGB2"
/replace="g"
/replace="t"
/db_xref="dbSNP:377550014"
variation 622
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:573468238"
variation 623
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318537464"
variation 624
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1321674757"
variation 627
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770511936"
variation 628
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759465267"
variation 629
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:371049621"
variation 630
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:1224627287"
variation 631
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:760611871"
variation 632
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362997198"
variation 633..638
/gene="CGB2"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:780705864"
variation 633
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:540962781"
variation 634
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:750724523"
variation 635
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252175982"
variation 636
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122135778"
variation 637
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758523378"
variation 638
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200008626"
variation 641
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751614145"
variation 645
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:200930560"
variation 646
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1234321908"
variation 647..648
/gene="CGB2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:745327270"
variation 647
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039765588"
variation 648
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039765670"
variation 649
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:781558432"
variation 650..652
/gene="CGB2"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1568657648"
variation 650
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1059305"
variation 652
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039765868"
variation 654
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412918115"
variation 655
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:770189990"
variation 656
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039765997"
variation 657
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202133130"
variation 658
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770509172"
variation 659
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773852875"
variation 660
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:758972659"
variation 662
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772040659"
variation 663
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1374370941"
variation 664
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248147513"
variation 665
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775624646"
variation 669
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:563497383"
variation 671
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:753717837"
variation 673
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:763186401"
variation 674
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:766526327"
variation 676..679
/gene="CGB2"
/replace="acac"
/replace="acacac"
/db_xref="dbSNP:769624942"
variation 676
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1600220838"
variation 677
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:531035587"
variation 679..682
/gene="CGB2"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:775720135"
variation 679
/gene="CGB2"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1014954743"
variation 680
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:751595129"
variation 681
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1373697554"
variation 682
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413645086"
variation 683
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755083053"
variation 686
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172541024"
variation 687
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039767177"
variation 688
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600220876"
variation 690
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1470111522"
variation 691
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355182438"
variation 692
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781657887"
variation 693
/gene="CGB2"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039767354"
regulatory 694..699
/regulatory_class="polyA_signal_sequence"
/gene="CGB2"
/note="hexamer: AATAAA"
variation 694
/gene="CGB2"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329538280"
variation 695
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:549468046"
variation 696
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1454338129"
variation 697
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450244941"
variation 700
/gene="CGB2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756642481"
variation 702
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:994527785"
variation 705
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226118495"
variation 707..714
/gene="CGB2"
/replace=""
/replace="caatccgc"
/db_xref="dbSNP:1209752653"
variation 707
/gene="CGB2"
/replace=""
/replace="c"
/db_xref="dbSNP:749096000"
variation 707
/gene="CGB2"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568657731"
variation 708..709
/gene="CGB2"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1568657738"
variation 708
/gene="CGB2"
/replace="a"
/replace="c"
/db_xref="dbSNP:1307550978"
variation 709
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:778059636"
variation 711..712
/gene="CGB2"
/replace="c"
/replace="cc"
/db_xref="dbSNP:543759521"
variation 711
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:952657324"
variation 712
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374106963"
variation 713
/gene="CGB2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770548953"
variation 714
/gene="CGB2"
/replace="c"
/replace="t"
/db_xref="dbSNP:778495999"
polyA_site 715
/gene="CGB2"
/note="major polyA site"
variation 715
/gene="CGB2"
/replace="a"
/replace="g"
/db_xref="dbSNP:745368260"
ORIGIN
gccctgcgttccgtggcgccccctggagggaggaaggggaactgtatctgagagagagcagccaattgggtccgctgactccggccgggttcccgtgccgcgtccaacacccctcactccctgtctcactcccccacggagactcaatttactttccatgtccacatccccagtgcttgcggaagatatcccgctaagagagagacatgtcaaaggggctgctgctgttgctgctgctgagcatgggcgggacatgggcatccaaggagccgcttcggccacggtgccgccccatcaatgccaccctggctgtggagaaggagggctgccccgtgtgcatcaccgtcaacaccaccatctgtgccggctactgccccaccatgacccgcgtgctgcagggggtcctgccggccctgcctcaggtggtgtgcaactaccgcgatgtgcgcttcgagtccatccggctccctggctgcccgcgcggcgtgaaccccgtggtctcctacgccgtggctctcagctgtcaatgtgcactctgccgccgcagcaccactgactgcgggggtcccaaggaccaccccttgacctgtgatgacccccgcttccaggcctcctcttcctcaaaggcccctccccccagccttccaagcccatcccgactcccggggccctcagacaccccgatcctcccacaataaaggcttctcaatccgca
//
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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