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Previous release (v1)
2024-05-19 11:06:11, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001382421 870 bp mRNA linear PRI 29-DEC-2022
DEFINITION Homo sapiens chorionic gonadotropin subunit beta 1 (CGB1),
transcript variant 2, mRNA.
ACCESSION NM_001382421
VERSION NM_001382421.1
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 870)
AUTHORS Wu W, Gao H, Li X, Peng S, Yu J, Liu N, Zhan G, Zhu Y, Wang K and
Guo X.
TITLE beta-hCG promotes epithelial ovarian cancer metastasis through
ERK/MMP2 signaling pathway
JOURNAL Cell Cycle 18 (1), 46-59 (2019)
PUBMED 30582718
REMARK GeneRIF: these data provide new insight into the roles and
mechanisms of b-hCG in regulating Epithelial ovarian cancer (EOC
metastasis through ERK/MMP2 signaling pathway and may become a new
target for therapeutic intervention.
REFERENCE 2 (bases 1 to 870)
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 3 (bases 1 to 870)
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 4 (bases 1 to 870)
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 5 (bases 1 to 870)
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 6 (bases 1 to 870)
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 870)
AUTHORS Jameson JL and Lindell CM.
TITLE Isolation and characterization of the human chorionic gonadotropin
beta subunit (CG beta) gene cluster: regulation of
transcriptionally active CG beta gene by cyclic AMP
JOURNAL Mol Cell Biol 8 (12), 5100-5107 (1988)
PUBMED 2468994
REFERENCE 8 (bases 1 to 870)
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 9 (bases 1 to 870)
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 10 (bases 1 to 870)
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
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AC008687.5.
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 CGB1 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 155
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 :: BC107144.1, ERR3218374.678556.1
[ECO:0000332]
RNAseq introns :: partial sample support SAMEA2162568
[ECO:0000350]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-370 AC008687.5 47834-48203 c
371-538 AC008687.5 47444-47611 c
539-870 AC008687.5 46877-47208 c
FEATURES Location/Qualifiers
source 1..870
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19q13.33"
gene 1..870
/gene="CGB1"
/note="chorionic gonadotropin subunit beta 1"
/db_xref="GeneID:114335"
/db_xref="HGNC:HGNC:16721"
/db_xref="MIM:608823"
exon 1..370
/gene="CGB1"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231819631"
variation 3
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:536700356"
variation 4
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1488096349"
variation 6
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:569421954"
variation 7
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039828600"
variation 8
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:551501295"
variation 9
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1262313547"
variation 10
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:532769722"
variation 11
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1162522223"
variation 12..13
/gene="CGB1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1308150352"
variation 12
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039828465"
variation 13..18
/gene="CGB1"
/replace="agggga"
/replace="aggggagggga"
/db_xref="dbSNP:202189266"
variation 13..14
/gene="CGB1"
/replace="ag"
/replace="agtggag"
/db_xref="dbSNP:1290022585"
variation 13
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:185491599"
variation 14..17
/gene="CGB1"
/replace="gggg"
/replace="ggggcgggg"
/db_xref="dbSNP:2122150436"
variation 14
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:900948651"
variation 15
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:942506736"
variation 17
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1372541577"
variation 20
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048265754"
variation 22
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:929929757"
variation 23
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:575971914"
variation 24
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039828117"
variation 25
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039828094"
variation 26
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:377385500"
variation 27
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:919258507"
variation 28..36
/gene="CGB1"
/replace="gagagag"
/replace="gagagagag"
/replace="gagagagagag"
/db_xref="dbSNP:1185637314"
variation 28
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122150376"
variation 30
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:972497937"
variation 32
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039827959"
variation 33
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600224459"
variation 34
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1386376438"
variation 35
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:960808642"
variation 36
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:868818970"
variation 37
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039827755"
variation 38
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:928009459"
variation 43
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:980898105"
variation 44
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:969506134"
variation 45
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1405321829"
variation 48
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1159195121"
variation 51
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:34291483"
variation 52
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:373044257"
variation 53
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:34228596"
variation 54
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:956980716"
variation 55
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1030646237"
variation 56
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1198195794"
variation 58
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039827242"
variation 59
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345735543"
variation 60..61
/gene="CGB1"
/replace=""
/replace="tg"
/db_xref="dbSNP:1555806967"
variation 60
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:10853805"
variation 61..62
/gene="CGB1"
/replace=""
/replace="gg"
/db_xref="dbSNP:1555806966"
variation 61
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039827098"
variation 62
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:35533886"
variation 63
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:900856459"
variation 64
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039826914"
variation 65
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:369471697"
variation 67
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1006650939"
variation 71
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:571679811"
variation 72
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451977649"
variation 73
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:182402915"
variation 74
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039826679"
variation 75
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1048255288"
variation 76
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039826622"
variation 77
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1211192571"
variation 78
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1327253886"
variation 79
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:929877689"
variation 80
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:377556920"
variation 81
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231941928"
variation 82
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1326505487"
variation 86
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039826427"
variation 87
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039826399"
variation 88
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373088178"
variation 89
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380971474"
variation 90
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039826306"
variation 91
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1340305554"
variation 95
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313831281"
variation 96
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:897107347"
variation 98
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039826183"
variation 101..112
/gene="CGB1"
/replace="gtctcactcccc"
/replace="gtctcactccccgtctcactcccc"
/db_xref="dbSNP:1462610580"
variation 101
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039826154"
variation 103
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1348503251"
variation 104
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1057060606"
variation 106
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1436845047"
variation 110
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1270624555"
variation 111
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:191756795"
variation 112
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369942258"
variation 113
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1600224361"
variation 115
/gene="CGB1"
/replace=""
/replace="c"
/db_xref="dbSNP:1600224356"
variation 115
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600224353"
variation 116
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:573599743"
variation 119
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:373660013"
variation 120
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:774444681"
variation 121
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039825739"
variation 122
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1466780913"
variation 123
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:375233005"
variation 124
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:927988907"
variation 127
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:981230197"
variation 130
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371968536"
variation 134
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:34566775"
variation 135
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:569543184"
variation 136
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039825520"
variation 137
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:377327911"
variation 139
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039825446"
variation 141
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039825429"
variation 143
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192328032"
variation 144
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766762733"
variation 146
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:541595731"
variation 147
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039825289"
variation 149
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751016313"
variation 150
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1484721212"
variation 152
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:766140640"
variation 153
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039825169"
variation 154
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031649274"
variation 155
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1648715505"
variation 157
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1240170111"
variation 158
/gene="CGB1"
/replace="c"
/replace="ccc"
/db_xref="dbSNP:2122149797"
variation 158
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260481965"
variation 159
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:762625218"
variation 160
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:373873835"
variation 162
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:769475713"
variation 164
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233529193"
variation 165
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:765647516"
variation 166
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568660258"
variation 167
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:186958845"
variation 168..170
/gene="CGB1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2039824813"
variation 168
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:777235070"
variation 170
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1382985885"
variation 171
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:769039759"
variation 173
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775492190"
variation 174..175
/gene="CGB1"
/replace=""
/replace="aa"
/db_xref="dbSNP:1332199875"
variation 176
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215113238"
variation 179
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772289035"
variation 180
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746052565"
variation 181
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777570430"
variation 182
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378558958"
variation 184
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039824503"
variation 185
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1201548329"
variation 187
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1233593844"
variation 188
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:769630365"
variation 190
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1568660224"
variation 192
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:375110238"
variation 193..194
/gene="CGB1"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1488968276"
variation 193
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781245225"
variation 196
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1277637999"
variation 197
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:754810554"
variation 198
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1303726020"
variation 200
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:751081848"
variation 204
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1276555275"
variation 204
/gene="CGB1"
/replace="t"
/replace="tt"
/db_xref="dbSNP:767091827"
variation 205
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1568660206"
variation 206
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:113383936"
variation 207
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039823877"
variation 209
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377394615"
variation 210
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039823829"
variation 213
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1325659012"
variation 214
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:759076930"
variation 215
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375604106"
variation 217
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:764951320"
variation 220
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1316179512"
variation 224
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1297346629"
variation 225
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039823643"
variation 226
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1400881482"
variation 227
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1292462701"
variation 228
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:762305269"
variation 229
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1006593052"
variation 233
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:34161060"
variation 234
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:764676756"
variation 235
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039823428"
variation 236
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600224192"
variation 237
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039823375"
variation 238
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:761022684"
variation 239
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1174852271"
variation 240
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775580246"
variation 242
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:772093173"
variation 244
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1193907628"
variation 245
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:528757170"
variation 246
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1026763373"
variation 249
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1650055812"
variation 251
/gene="CGB1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2039823142"
variation 251
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187791620"
variation 252
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165556788"
variation 254
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039823055"
variation 255
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:368649819"
variation 257
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:897003433"
variation 258
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1057398455"
variation 262
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:878892026"
variation 263
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600224170"
variation 265
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1160356390"
variation 266
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039822875"
variation 267
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039822851"
variation 272
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600224166"
variation 273
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039822788"
variation 274
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122149299"
variation 275
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:139808007"
variation 276
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420234375"
variation 277
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039822647"
variation 279
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1186410500"
variation 280
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039822602"
variation 282
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438009657"
variation 283
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353353562"
variation 284
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1416370144"
variation 285
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:574454338"
variation 286
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1045108837"
variation 287
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039822465"
variation 288
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1236328530"
variation 290
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039822423"
variation 293
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280801395"
variation 294
/gene="CGB1"
/replace=""
/replace="c"
/db_xref="dbSNP:1350686905"
variation 295
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039822351"
misc_feature 296..298
/gene="CGB1"
/note="upstream in-frame stop codon"
variation 297
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:769456885"
variation 302
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039822307"
variation 303
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:948098576"
variation 304
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1196269279"
variation 305..306
/gene="CGB1"
/replace=""
/replace="t"
/db_xref="dbSNP:548402220"
variation 305
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:182231647"
variation 306
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039822160"
variation 307
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1235615248"
variation 308
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1184168510"
variation 309
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1364490817"
variation 310
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:915355832"
variation 311
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039822030"
variation 312
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:556529036"
variation 313
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:935448906"
variation 314
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039821934"
variation 317
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1240055975"
variation 319
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039821860"
variation 320
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371352309"
variation 323
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:977402261"
variation 324
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:559439811"
variation 325
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:187212872"
variation 329
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2122149080"
variation 331
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1337806383"
variation 332
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1329525188"
variation 333
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568660097"
variation 334
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364789325"
variation 336
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039821618"
variation 337..339
/gene="CGB1"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:2039821586"
variation 342
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:541425169"
variation 345
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039821518"
variation 346
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039821494"
variation 348
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232883419"
variation 349
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:910861384"
variation 350
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235580692"
variation 352
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039821405"
variation 354
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:112028365"
variation 356
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039821337"
variation 358
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:561627652"
variation 360
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039821289"
variation 362
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1197799616"
variation 364
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039821226"
variation 369
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039821195"
exon 371..538
/gene="CGB1"
/inference="alignment:Splign:2.1.0"
variation 371
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:62126040"
variation 372
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1457305022"
variation 373
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:746779481"
variation 374
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1311038616"
variation 377
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1200221979"
variation 378..388
/gene="CGB1"
/replace="tgctgttgctg"
/replace="tgctgttgctgttgctg"
/db_xref="dbSNP:765624542"
variation 379
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1332430658"
variation 380
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:572197136"
variation 382
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1228003059"
variation 384
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270512752"
variation 385
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357119887"
variation 387
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039816765"
variation 388
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039816692"
variation 392
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:775626611"
variation 396
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:772131200"
variation 397
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332650382"
CDS 398..829
/gene="CGB1"
/note="isoform 2 is encoded by transcript variant 2;
chorionic gonadotropin, beta polypeptide 1; chorionic
gonadotropin beta subunit 1"
/codon_start=1
/product="choriogonadotropin subunit beta variant 1
isoform 2"
/protein_id="NP_001369350.1"
/db_xref="GeneID:114335"
/db_xref="HGNC:HGNC:16721"
/db_xref="MIM:608823"
/translation="
MGGTWASKEPLRPRCRPINATLAVEKEGCPVCITVNTTICAGYCPTMTRVLQGVLPALPQVVCNYRDVRFESIRLPGCPRGVNPVVSYAVALSCQCALCRRSTTDCGGPKDHPLTCDDPRFQDSSSSKAPPPSLPSPSRLPGP"
misc_feature 428..748
/gene="CGB1"
/note="Glycoprotein hormone beta chain homologues; Region:
GHB; smart00068"
/db_xref="CDD:214502"
misc_feature order(440..442,515..517,527..529,584..586,677..679,
683..685)
/gene="CGB1"
/note="cysteine knot motif; other site"
/db_xref="CDD:200450"
misc_feature order(461..463,470..472,512..553,581..586,692..694,
698..700,707..724)
/gene="CGB1"
/note="dimer interface [polypeptide binding]; other site"
/db_xref="CDD:200450"
misc_feature order(551..553,698..703,710..712,716..724)
/gene="CGB1"
/note="receptor binding site [polypeptide binding]; other
site"
/db_xref="CDD:200450"
variation 399
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745374910"
variation 400
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402369392"
variation 401
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:147731004"
variation 403
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1322428206"
variation 404
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304075768"
variation 407
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748849664"
variation 410
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600223869"
variation 412
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415312784"
variation 413
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:553812864"
variation 415
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:756480507"
variation 417
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380774679"
variation 418
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:768020387"
variation 419
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:755423976"
variation 420
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145503774"
variation 421
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:574448905"
variation 424
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452477184"
variation 425
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1185137906"
variation 426
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773355851"
variation 427
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:200371312"
variation 431
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164418301"
variation 432
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:760613888"
variation 433
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039815790"
variation 434
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1310586210"
variation 435
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039815729"
variation 438
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1463048562"
variation 439
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242993940"
variation 440
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2122147489"
variation 441
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772147750"
variation 443
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1274689310"
variation 444
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:745750183"
variation 445
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187529607"
variation 447
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039815499"
variation 450
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2122147444"
variation 451
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351190630"
variation 452
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315800817"
variation 453
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:773940761"
variation 458
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600223835"
variation 459
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:202067695"
variation 460
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429863566"
variation 462
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:770384780"
variation 464
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1268216650"
variation 465
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:556214869"
variation 468
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:777344526"
variation 470
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:537693352"
variation 471..475
/gene="CGB1"
/replace="ag"
/replace="agaag"
/db_xref="dbSNP:759938269"
variation 471
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1478896026"
variation 472
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039815089"
variation 476
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1555806873"
variation 479
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:570339247"
variation 480
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1291309081"
variation 481
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148640164"
variation 483
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487983670"
variation 485
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755513430"
variation 486
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1219412279"
variation 487
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:752048144"
variation 488
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:766888572"
variation 489
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:758466573"
variation 492
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415924632"
variation 496..511
/gene="CGB1"
/replace="cacc"
/replace="caccgtcaacaccacc"
/db_xref="dbSNP:777177662"
variation 496
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:750513213"
variation 499
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765381688"
variation 505..512
/gene="CGB1"
/replace="cacca"
/replace="caccacca"
/db_xref="dbSNP:1480444426"
variation 505
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399064983"
variation 507
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762069467"
variation 508
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:752562285"
variation 509
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:767378543"
variation 510
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:759370769"
variation 511
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:889943275"
variation 512
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1176736924"
variation 514
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:774201663"
variation 517
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1417184280"
variation 518
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039814294"
variation 519
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:770884058"
variation 520
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1477649626"
variation 521
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1263989867"
variation 522
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1195851629"
variation 523
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1400360575"
variation 527
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1482324192"
variation 528
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:762432991"
variation 529
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211475929"
variation 530
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284292258"
variation 531
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1049923872"
variation 533
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039813919"
variation 534
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:558208220"
variation 535
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:540021521"
variation 536
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1256625036"
variation 537
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769462042"
variation 538
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:747762967"
exon 539..870
/gene="CGB1"
/inference="alignment:Splign:2.1.0"
variation 541
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1458468311"
variation 542
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1240464080"
variation 543
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600223510"
variation 544
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:940301796"
variation 545
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039809609"
variation 546
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207689861"
variation 547
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:747339118"
variation 551
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039809517"
variation 552
/gene="CGB1"
/replace="a"
/replace="aa"
/db_xref="dbSNP:760737028"
variation 552
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045834630"
variation 553
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1245486233"
variation 554
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223057392"
variation 555
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350895730"
variation 556
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1917031560"
variation 557
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039809326"
variation 560
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285197170"
variation 564
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1308394303"
variation 565
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:541921440"
variation 566
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:574589925"
variation 568
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:556155690"
variation 569
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1054225655"
variation 570
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423857516"
variation 573
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039809103"
variation 576
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386013028"
variation 578
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:779529842"
variation 579
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039809016"
variation 582
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039808987"
variation 584
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1600223464"
variation 586
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1294362608"
variation 588
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:544218520"
variation 592
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039808877"
variation 593
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753951799"
variation 594
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1158546357"
variation 595
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:778204464"
variation 596
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446116331"
variation 598..611
/gene="CGB1"
/replace="t"
/replace="tgtgcgcttcgagt"
/db_xref="dbSNP:773175443"
variation 598
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576811185"
variation 600
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039808655"
variation 601
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039808625"
variation 602
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751337658"
variation 603
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1432984304"
variation 605
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039808507"
variation 607
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390883370"
variation 608
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758100273"
variation 612
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:750411436"
variation 614
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765148068"
variation 617
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371128021"
variation 618
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1284750505"
variation 619
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:776054068"
variation 623
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355681618"
variation 624
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:763750280"
variation 625
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1393292136"
variation 631..633
/gene="CGB1"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:772368413"
variation 633
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232195649"
variation 634
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1568659618"
variation 635
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331501646"
variation 636
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:539760342"
variation 637
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:775748503"
variation 640
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1180513505"
variation 641
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775053454"
variation 642
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1441666737"
variation 644
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246303905"
variation 646
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:566235393"
variation 647
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1379146170"
variation 649
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:756326891"
variation 650
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201312433"
variation 651
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:781251303"
variation 655
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465821820"
variation 658
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378616613"
variation 660
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1452013968"
variation 661
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750216960"
variation 662
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:765164331"
variation 664
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1262024856"
variation 665
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:377262139"
variation 669
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448244749"
variation 676
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253945854"
variation 678
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199839749"
variation 679
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345421914"
variation 680
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1197549618"
variation 682
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:753367928"
variation 683
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:535514659"
variation 684
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:568205173"
variation 685
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:987232053"
variation 686
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1179874353"
variation 687
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277824533"
variation 688
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1600223350"
variation 690
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:775256818"
variation 693
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039806754"
variation 695
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328312410"
variation 696
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:1332739331"
variation 697
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1345340610"
variation 698
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:767060656"
variation 699
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374210570"
variation 700
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039806573"
variation 702
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1600223341"
variation 703
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:774785916"
variation 705
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:771575126"
variation 706
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:749776099"
variation 708
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1600223327"
variation 709
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568659539"
variation 712
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:773829110"
variation 713
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039806292"
variation 715
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200177766"
variation 716
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748166776"
variation 720
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199498446"
variation 721
/gene="CGB1"
/replace="g"
/replace="t"
/db_xref="dbSNP:745677072"
variation 722
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039806119"
variation 723
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:778631969"
variation 724
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039806052"
variation 726
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1028339582"
variation 727
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:376922188"
variation 729
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:753813017"
variation 733
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:777548163"
variation 735
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219523475"
variation 740
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399939084"
variation 749
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:755706231"
variation 750
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:752141739"
variation 751..755
/gene="CGB1"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1276406376"
variation 751
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373128472"
variation 753
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766894199"
variation 755
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:763390923"
variation 756
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367977437"
variation 760
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773830373"
variation 761
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016217801"
variation 762
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:770198800"
variation 764
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:369301126"
variation 765
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:201231416"
variation 768
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039805299"
variation 770
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1247688792"
variation 771
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039805212"
variation 772
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:747191041"
variation 775
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039805157"
variation 776
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1162053395"
variation 778..780
/gene="CGB1"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1600223257"
variation 782
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1472850816"
variation 783
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780217968"
variation 784
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1388593246"
variation 785
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:375388018"
variation 786
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039804877"
variation 787
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039804837"
variation 788..793
/gene="CGB1"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1487932358"
variation 788
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:373307100"
variation 790
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1350290889"
variation 791
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755936073"
variation 792
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:752261004"
variation 793
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780516618"
variation 794
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1568659471"
variation 796
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200388907"
variation 797
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199785120"
variation 800
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:763481551"
variation 802
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2122145032"
variation 803
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:570788485"
variation 804
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765789272"
variation 805
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202114192"
variation 806
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1488200563"
variation 807
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776805155"
variation 808
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768762805"
variation 810
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347699604"
variation 811
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1568659444"
variation 812
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:527614195"
variation 813
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:772276702"
variation 814
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:370143488"
variation 817
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1156748774"
variation 818
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:35371968"
variation 819
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380679945"
variation 820..823
/gene="CGB1"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:2122144824"
variation 820
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748079220"
variation 821
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1476931130"
variation 822
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:781171716"
variation 823
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1198471026"
variation 824
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1490527489"
variation 827
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:754596236"
variation 828
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:200329830"
variation 829
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:542056595"
variation 830
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1285587786"
variation 834
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:758068882"
variation 836
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:755082872"
variation 837
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757610056"
variation 838
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1273850342"
variation 839
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:974126947"
variation 840
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754350682"
variation 842
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:529956719"
variation 843
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:1288631414"
variation 844
/gene="CGB1"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775477990"
variation 845
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:1295883640"
variation 846
/gene="CGB1"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039803190"
variation 848
/gene="CGB1"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767737637"
regulatory 849..854
/regulatory_class="polyA_signal_sequence"
/gene="CGB1"
/note="hexamer: AATAAA"
variation 850
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015752308"
variation 851
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:759624854"
variation 854
/gene="CGB1"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188343359"
variation 856
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:773087735"
variation 857
/gene="CGB1"
/replace="c"
/replace="t"
/db_xref="dbSNP:1412512140"
variation 861
/gene="CGB1"
/replace="a"
/replace="t"
/db_xref="dbSNP:769530205"
variation 867
/gene="CGB1"
/replace="c"
/replace="g"
/db_xref="dbSNP:747965736"
variation 868
/gene="CGB1"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:367968985"
variation 869
/gene="CGB1"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:562568855"
polyA_site 870
/gene="CGB1"
/note="major polyA site"
ORIGIN
ctggagggaggaaggggaactgcatctgagagagagcagccaattgggtccgctgactctggccaggttcccgtgccgcgtccaacacccctcactccctgtctcactcccccacggagactcaatttactttccatgtccacattcccagtgcttgcggaagatatcccgctaagagagagacatgtcaaaggtagggtagatccacatttccgggcaccaaagatggagatgttccaggaaagactgcagggcccctgggcaccttccacctccttccaggccatcactggcatgagaaggggcagacccgtgtgagctgtggaaggaggcctctttctggaggagcgtgacccccagtaagcttcagaggctgctgctgttgctgctgctgagcatgggcgggacatgggcatccaaggagccgcttcggccacggtgccgccccatcaatgccaccctggctgtggagaaggagggctgccccgtgtgcatcaccgtcaacaccaccatctgtgccggctactgccccaccatgacccgcgtgctgcagggggtcctgccggccctgcctcaggtggtgtgcaactaccgcgatgtgcgcttcgagtccatccggctccctggctgcccgcgcggcgtgaaccccgtggtctcctacgccgtggctctcagctgtcaatgtgcactctgccgccgcagcaccactgactgcgggggtcccaaggaccaccccttgacctgtgatgacccccgcttccaggactcctcttcctcaaaggcccctccccccagccttccaagtccatcccgtctcccggggccctaggacaccccgatcctcccacaataaaggcttctcaatccgca
//
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.
[Full Text]