2024-05-19 10:29:19, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_033183 887 bp mRNA linear PRI 08-JUN-2022 DEFINITION Homo sapiens chorionic gonadotropin subunit beta 8 (CGB8), mRNA. ACCESSION NM_033183 VERSION NM_033183.3 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 887) AUTHORS Bellet D, Lazar V, Bieche I, Paradis V, Giovangrandi Y, Paterlini P, Lidereau R, Bedossa P, Bidart JM and Vidaud M. TITLE Malignant transformation of nontrophoblastic cells is associated with the expression of chorionic gonadotropin beta genes normally transcribed in trophoblastic cells JOURNAL Cancer Res 57 (3), 516-523 (1997) PUBMED 9012484 REFERENCE 2 (bases 1 to 887) 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 3 (bases 1 to 887) 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 4 (bases 1 to 887) AUTHORS Otani T, Otani F, Krych M, Chaplin DD and Boime I. TITLE Identification of a promoter region in the CG beta gene cluster JOURNAL J Biol Chem 263 (15), 7322-7329 (1988) PUBMED 2452822 REMARK Erratum:[J Biol Chem 1988 Dec 15;263(35):19256-7] REFERENCE 5 (bases 1 to 887) AUTHORS Jameson,J.L., Lindell,C.M. and Habener,J.F. TITLE Evolution of different transcriptional start sites in the human luteinizing hormone and chorionic gonadotropin beta-subunit genes JOURNAL DNA 5 (3), 227-234 (1986) PUBMED 2424697 REFERENCE 6 (bases 1 to 887) 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 7 (bases 1 to 887) AUTHORS Talmadge,K., Boorstein,W.R., Vamvakopoulos,N.C., Gething,M.J. and Fiddes,J.C. TITLE Only three of the seven human chorionic gonadotropin beta subunit genes can be expressed in the placenta JOURNAL Nucleic Acids Res 12 (22), 8415-8436 (1984) PUBMED 6209613 REFERENCE 8 (bases 1 to 887) AUTHORS Talmadge,K., Vamvakopoulos,N.C. and Fiddes,J.C. TITLE Evolution of the genes for the beta subunits of human chorionic gonadotropin and luteinizing hormone JOURNAL Nature 307 (5946), 37-40 (1984) PUBMED 6690982 REFERENCE 9 (bases 1 to 887) 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 887) 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 BX118262.1, BC030994.1, BX380841.2 and BQ011275.1. On Feb 27, 2020 this sequence version replaced NM_033183.2. Summary: This gene is a member of the glycoprotein hormone beta chain family and encodes the beta 8 subunit of chorionic gonadotropin (CG). Glycoprotein hormones are heterodimers consisting of a common alpha subunit and an unique beta subunit which confers biological specificity. CG is produced by the trophoblastic cells of the placenta and stimulates the ovaries to synthesize the steroids that are essential for the maintenance of pregnancy. The beta subunit of CG is encoded by 6 genes which are arranged in tandem and inverted pairs on chromosome 19q13.3 and contiguous with the luteinizing hormone beta subunit gene. [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 :: BX336447.2, BX396345.2 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2162568 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000448456.4/ ENSP00000403649.2 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## COMPLETENESS: full length. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-5 BX118262.1 1-5 6-107 BC030994.1 1-102 108-265 BX380841.2 90-247 266-884 BC030994.1 261-879 885-887 BQ011275.1 18-20 c FEATURES Location/Qualifiers source 1..887 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="19" /map="19q13.33" gene 1..887 /gene="CGB8" /note="chorionic gonadotropin subunit beta 8" /db_xref="GeneID:94115" /db_xref="HGNC:HGNC:16453" /db_xref="MIM:608827" exon 1..387 /gene="CGB8" /inference="alignment:Splign:2.1.0" variation 1 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:927385106" variation 2 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2039968253" variation 6 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039968240" variation 7 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:527286201" variation 8 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:2039968205" variation 9 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1443586656" variation 15 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2039968174" variation 16 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1314591156" variation 19 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1288297077" variation 22 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1405429766" variation 23 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:559942017" variation 24 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1568401942" variation 25 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039968047" variation 26 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1600233828" variation 28 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1044538806" variation 29 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1289770844" variation 30 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1382350370" variation 35 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:541692276" variation 37 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1600233819" variation 39 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1600233817" variation 42 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1360333893" variation 43 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:947541503" variation 45 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:113708336" variation 46 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1600233805" variation 49 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:111755713" variation 50 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:914824403" variation 51 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1600233799" variation 52 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2039967776" variation 53 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:989096317" variation 54 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1460684445" variation 56 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1600233792" variation 57 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:955679024" variation 58 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2039967704" variation 60 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039967688" variation 61 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:2039967672" variation 63 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1451778138" variation 69 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039967659" variation 70 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1472845236" variation 73 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1387932903" variation 74 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1158372040" variation 76 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:2039967593" variation 82 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1480683078" variation 83 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1600233773" variation 84 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039967535" variation 85 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039967519" variation 86 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039967500" variation 89 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1431176580" variation 91 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1160512973" variation 92 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:369281397" variation 98 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1468554974" variation 99 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1338949652" variation 102 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:922986389" variation 103 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1461109804" variation 104 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039967354" variation 105 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:62127875" variation 106 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1277812338" variation 108 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:13345685" variation 109 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:964462686" variation 110 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1266866956" variation 111 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039967203" variation 113 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1017780004" variation 114 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039967167" variation 116 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039967151" variation 118 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1326356525" variation 119 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:2039967117" variation 121 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039967097" variation 122 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2039967079" variation 124 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1322629709" variation 126 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:373833236" variation 127 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1233040788" variation 129 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1026178280" variation 130 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1298032994" variation 132 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1470866917" variation 133 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:2039966933" variation 134 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1183609918" variation 135 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1380707573" variation 137 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1178968969" variation 139 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1600233704" variation 141 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:555967253" variation 142 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1409650202" variation 144 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039966795" variation 145 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:866992263" variation 146 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1470990358" variation 149 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2039966722" variation 150..151 /gene="CGB8" /replace="" /replace="tt" /db_xref="dbSNP:2039966691" variation 150 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039966707" variation 153 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1408296107" variation 155 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:544044327" variation 156 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:868175758" variation 159 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039966607" variation 163 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1284921968" variation 164 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1170709314" variation 165 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1057104896" variation 171 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:576563791" variation 172 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1373391290" variation 176 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1600233655" variation 177 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1600233653" variation 178 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:868015801" variation 179 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:905910161" variation 182 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1202186607" variation 183 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1044541698" variation 185 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1447222494" variation 187 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2039966411" variation 188 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1247014908" variation 190 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039966372" variation 192 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039966354" variation 193 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1183736181" variation 195 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:558235037" variation 197 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:947528887" variation 198 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2039966266" variation 199 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1462241730" variation 200 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1254741719" variation 201 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:539594872" variation 202 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2039966175" variation 204 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039966165" variation 205 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1325420259" variation 208 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1340542443" variation 209 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1253381999" variation 210 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1268052400" variation 213 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:914773420" variation 214 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1225540156" variation 215 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1290452117" variation 216 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1341793603" variation 217 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1315990221" variation 220 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:566056058" variation 222 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1225436649" variation 223 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1380647478" variation 225..238 /gene="CGB8" /replace="cctg" /replace="cctgcgcccccctg" /db_xref="dbSNP:1389206681" variation 225 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1600233610" variation 226 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1268659380" variation 229 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:553913141" variation 230 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1395317247" variation 231..236 /gene="CGB8" /replace="ccccc" /replace="cccccc" /replace="ccccccc" /db_xref="dbSNP:1053347001" variation 231 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1450285153" variation 233 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1396963008" variation 234 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1169488157" variation 235 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039965759" variation 236 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1427574127" variation 237 /gene="CGB8" /replace="" /replace="t" /db_xref="dbSNP:2039965701" variation 237 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1391282608" variation 238 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1315911368" variation 240 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:535343785" variation 244 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1600233574" variation 245 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1600233571" variation 250 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:750405784" variation 252 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:923531003" variation 254 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:778523474" variation 255 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1356725899" variation 256..261 /gene="CGB8" /replace="ccccc" /replace="cccccc" /replace="ccccccc" /db_xref="dbSNP:1366164738" variation 256 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1459529823" variation 257 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:964734837" variation 258 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2039965479" variation 259 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1350532012" variation 261 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:910299776" variation 262 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1241527122" variation 263 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:2039965358" variation 264 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1187470734" variation 265..267 /gene="CGB8" /replace="ggg" /replace="gggg" /db_xref="dbSNP:2039965283" variation 265 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:568037183" variation 266 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1438843473" variation 270 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:549532359" variation 271 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039965244" variation 273 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:866060952" variation 275 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:951866166" variation 276 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:993307048" variation 278 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039965159" variation 282 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1335674645" variation 283 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039965115" variation 284 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:191081201" variation 286 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1397289989" variation 289 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039965066" variation 290 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:375056743" variation 291 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1600233502" variation 292 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1248397278" variation 293 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:960624113" variation 296 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1270564690" variation 297 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:573446384" variation 300 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039964953" variation 301 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:35930240" variation 304 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039964890" variation 310 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:552249701" variation 312..313 /gene="CGB8" /replace="t" /replace="tt" /db_xref="dbSNP:2039964855" variation 313 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:2039964841" variation 315 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2039964815" variation 316 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:527438751" variation 317 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1249965616" variation 318 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039964765" variation 320 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039964748" variation 322 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1413193902" variation 323 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1178539999" variation 324 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039964680" variation 325 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:778138392" variation 326 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1472803002" variation 327..330 /gene="CGB8" /replace="ccc" /replace="cccc" /db_xref="dbSNP:760060947" variation 327 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:560069731" variation 328 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1600233461" variation 329 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039964588" variation 330 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:781444161" variation 331 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:755157129" variation 334 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039964495" variation 335 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:751625982" variation 336 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1058676" misc_feature 337..339 /gene="CGB8" /note="upstream in-frame stop codon" variation 338..340 /gene="CGB8" /replace="aa" /replace="aaa" /db_xref="dbSNP:776538441" variation 338 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:758635357" variation 340 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:753589540" variation 341 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:763810383" variation 342 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1290763938" variation 343 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:760641309" variation 344 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:752586487" variation 345..346 /gene="CGB8" /replace="g" /replace="gg" /db_xref="dbSNP:905895150" variation 346 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:767422941" variation 348 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2039964245" variation 349 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:773895792" variation 350 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1437360199" variation 351 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:3179073" variation 352 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:373970115" variation 356 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:773739423" variation 357 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039964108" variation 361 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:200172544" variation 363 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1483317921" variation 364 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:3179074" variation 365 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1486620019" variation 367 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:748500709" variation 368 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:369852403" variation 371 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2039963944" variation 372 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:562375956" CDS 373..870 /gene="CGB8" /note="chorionic gonadotropin beta 8 subunit; chorionic gonadotropin, beta polypeptide 8; chorionic gonadotropin beta subunit 8" /codon_start=1 /product="chorionic gonadotropin, beta polypeptide 8 precursor" /protein_id="NP_149439.1" /db_xref="CCDS:CCDS12753.1" /db_xref="GeneID:94115" /db_xref="HGNC:HGNC:16453" /db_xref="MIM:608827" /translation="
MEMFQGLLLLLLLSMGGTWASKEPLRPRCRPINATLAVEKEGCPVCITVNTTICAGYCPTMTRVLQGVLPALPQVVCNYRDVRFESIRLPGCPRGVNPVVSYAVALSCQCALCRRSTTDCGGPKDHPLTCDDPRFQDSSSSKAPPPSLPSPSRLPGPSDTPILPQ"
sig_peptide 373..432 /gene="CGB8" /inference="COORDINATES: ab initio prediction:SignalP:4.0" mat_peptide 433..867 /gene="CGB8" /product="chorionic gonadotropin, beta polypeptide 8" misc_feature 445..765 /gene="CGB8" /note="Glycoprotein hormone beta chain homologues; Region: GHB; smart00068" /db_xref="CDD:214502" misc_feature order(457..459,532..534,544..546,601..603,694..696, 700..702) /gene="CGB8" /note="cysteine knot motif; other site" /db_xref="CDD:200450" misc_feature order(478..480,487..489,529..570,598..603,709..711, 715..717,724..741) /gene="CGB8" /note="dimer interface [polypeptide binding]; other site" /db_xref="CDD:200450" misc_feature order(568..570,715..720,727..729,733..741) /gene="CGB8" /note="receptor binding site [polypeptide binding]; other site" /db_xref="CDD:200450" variation 373 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039963900" variation 374 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039963879" variation 376 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039963843" variation 379 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:2039963829" variation 380 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:543985594" variation 381 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:779504396" variation 382 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:375079954" variation 384 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:777570407" variation 386 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2039963682" variation 387 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:755955723" exon 388..555 /gene="CGB8" /inference="alignment:Splign:2.1.0" variation 388 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1480973610" variation 389 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:200252416" variation 390..411 /gene="CGB8" /replace="gctgctgctg" /replace="gctgctgctgttgctgctgctg" /db_xref="dbSNP:2039959624" variation 390 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:879314125" variation 393 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1321695079" variation 396 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039959762" variation 397 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:566523170" variation 399 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1235600899" variation 401..411 /gene="CGB8" /replace="tgctgctg" /replace="tgctgctgctg" /db_xref="dbSNP:773474816" variation 402 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1349018833" variation 407 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1301885123" variation 409 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1306959729" variation 411 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039959578" variation 414 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1391632805" variation 415 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039959547" variation 419 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1397957461" variation 420 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1291338428" variation 421 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:939188673" variation 423 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1418576610" variation 424 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1226978080" variation 427 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1600233096" variation 435 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039959410" variation 437 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:4002414" variation 442 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:4002413" variation 443 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:3956248" variation 444 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:151241744" variation 445 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1201056256" variation 446 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1333717539" variation 448 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:548297904" variation 449..450 /gene="CGB8" /replace="g" /replace="gg" /db_xref="dbSNP:1315545201" variation 449 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1252727580" variation 450 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1208197065" variation 451 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1472793235" variation 452 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1488437514" variation 454 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1274277359" variation 455 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1375512783" variation 456 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1216108589" variation 459 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1327459676" variation 460 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1288148952" variation 461 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:200193894" variation 462..465 /gene="CGB8" /replace="ccc" /replace="cccc" /db_xref="dbSNP:1337225352" variation 462 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1310377685" variation 463 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039958861" variation 466 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1351564806" variation 468 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:927811511" variation 470 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1298558119" variation 471 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1299488520" variation 474 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1440203801" variation 476..478 /gene="CGB8" /replace="cc" /replace="ccc" /db_xref="dbSNP:2039958656" variation 476 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:201642487" variation 477 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1395534002" variation 480 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039958634" variation 482 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039958608" variation 492 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039958586" variation 493 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1385671877" variation 494 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:1394599735" variation 500 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1328223631" variation 501 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1327780746" variation 503 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1455605923" variation 504 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:201210467" variation 505 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:969683335" variation 508 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1470626289" variation 509 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:2039958399" variation 511 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1365834346" variation 513 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039958349" variation 516 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1197028833" variation 517 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:879504409" variation 524 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1253724360" variation 525 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039958223" variation 526 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:2039958188" variation 527 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1409994674" variation 533 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1389083518" variation 534 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039958080" variation 537 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1196002497" variation 538 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1171045388" variation 540 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039957974" variation 543 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039957955" variation 547 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2039957925" variation 548 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1371653075" variation 551 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039957899" variation 552 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1292184870" variation 553 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1463964361" variation 554 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1387617817" variation 555 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1297135387" exon 556..887 /gene="CGB8" /inference="alignment:Splign:2.1.0" variation 557 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039955854" variation 558 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1395836862" variation 559 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1449050206" variation 560 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039955778" variation 561 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1254549069" variation 562 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1368576109" variation 564 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2122181030" variation 567 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1395219675" variation 569 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:2039955692" variation 570 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039955667" variation 572 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1199499010" variation 573 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1036094024" variation 574 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1281823013" variation 575 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1944767095" variation 581 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1225630375" variation 582 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1340849580" variation 583 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1270636255" variation 585 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039955500" variation 590 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1432830344" variation 593 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1305171006" variation 595 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1338439169" variation 596 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1226955747" variation 597 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1296076388" variation 599 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:1426373974" variation 604 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1333304750" variation 605 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1414372486" variation 609 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039955318" variation 610 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:939075476" variation 611 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:927750169" variation 612 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1045268348" variation 613 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039955199" variation 616 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1448961248" variation 618 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1186705800" variation 619 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039955111" variation 620 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1278607726" variation 622 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1392065675" variation 624 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2039955053" variation 625 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1427842368" variation 629 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1418927544" variation 630 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039954995" variation 634 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1168957964" variation 635 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1476698050" variation 636 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1367065908" variation 639 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1327519466" variation 642 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:2039954893" variation 643 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039954869" variation 645 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1394708541" variation 650 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:879871530" variation 651 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1327661855" variation 652 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1485790538" variation 653 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1259097854" variation 654 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1202604631" variation 655 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:947869967" variation 656 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1273130331" variation 657 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1216223463" variation 658 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1354221277" variation 662 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:2039954579" variation 663 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039954560" variation 664 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039954536" variation 665 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1207032987" variation 666 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039954497" variation 667 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1250045233" variation 672 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1447653155" variation 673 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:2039954432" variation 675 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1193818335" variation 678 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1283378606" variation 679 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1233608301" variation 681 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1357154168" variation 682 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1314950555" variation 685 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039954304" variation 692 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039954288" variation 693 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1418273120" variation 697 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1408268108" variation 698 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:761501379" variation 699 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:777142528" variation 703 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1318112651" variation 704 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2039954160" variation 706 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039954144" variation 712 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2039954129" variation 713 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1386494839" variation 715 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2039954086" variation 716 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1412121230" variation 718 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1371966649" variation 722 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1334109169" variation 724 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:1339184514" variation 732 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:764479656" variation 733 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1568401450" variation 736 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1600232748" variation 737 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:2039953947" variation 738 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1600232745" variation 744 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1164838453" variation 745..746 /gene="CGB8" /replace="" /replace="c" /db_xref="dbSNP:2039953883" variation 745 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039953893" variation 746 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:915158482" variation 747 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1328892565" variation 750..753 /gene="CGB8" /replace="ccc" /replace="cccc" /db_xref="dbSNP:2039953788" variation 752 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1420501659" variation 753 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1179514938" variation 755..769 /gene="CGB8" /replace="tgacc" /replace="tgacctgtgatgacc" /db_xref="dbSNP:1199896923" variation 758 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1469342009" variation 768 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2122180563" variation 769 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1232927270" variation 770 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1555730639" variation 772 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1255429765" variation 773 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:761108717" variation 774 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1449384016" variation 779 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1258039073" variation 782 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:71352727" variation 783 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039953583" variation 785 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1214273774" variation 786 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039953489" variation 787 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:560353315" variation 790 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:1336631374" variation 791 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:989431114" variation 792 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1194178298" variation 793 /gene="CGB8" /replace="" /replace="t" /db_xref="dbSNP:1453890887" variation 793 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:957345376" variation 794 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:772432114" variation 797 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:1222259857" variation 798..799 /gene="CGB8" /replace="g" /replace="gg" /db_xref="dbSNP:1313951173" variation 798 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:924628224" variation 799 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1280203641" variation 800 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1251940371" variation 801 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039953201" variation 803 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:2122180404" variation 805 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1444382562" variation 806 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1348219257" variation 807 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039953172" variation 809 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:746017552" variation 810 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1059301" variation 812 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:771144380" variation 813 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1397097432" variation 814 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1213024951" variation 819 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:1280942665" variation 821 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039953027" variation 822 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:71352726" variation 823 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1399740701" variation 828 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:780868130" variation 829 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:977466134" variation 830 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1389582639" variation 831 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:1476729892" variation 832 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:966494961" variation 834 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1428264035" variation 836 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:754850276" variation 837 /gene="CGB8" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:541914599" variation 838 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1386432763" variation 839 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1299465562" variation 840 /gene="CGB8" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1235091171" variation 841 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1469806843" variation 842 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039952723" variation 843 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1600232631" variation 845 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1265993895" variation 846 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:17846297" variation 847 /gene="CGB8" /replace="g" /replace="t" /db_xref="dbSNP:1252869957" variation 850 /gene="CGB8" /replace="a" /replace="t" /db_xref="dbSNP:2039952612" variation 852 /gene="CGB8" /replace="a" /replace="c" /db_xref="dbSNP:1480798531" variation 853 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1317298049" variation 854 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:758253561" variation 855 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:749968106" variation 856 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:764775385" variation 859 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:2039952483" variation 865 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1302813895" regulatory 866..871 /regulatory_class="polyA_signal_sequence" /gene="CGB8" /note="hexamer: AATAAA" variation 867 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:953583126" variation 872..873 /gene="CGB8" /replace="g" /replace="gg" /db_xref="dbSNP:2039952438" variation 873 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1442250006" variation 877 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:2039952399" variation 879 /gene="CGB8" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:2039952381" variation 881 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:2039952364" variation 883 /gene="CGB8" /replace="c" /replace="g" /db_xref="dbSNP:1373899318" variation 884 /gene="CGB8" /replace="c" /replace="t" /db_xref="dbSNP:1318950539" variation 885 /gene="CGB8" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:995076835" variation 886 /gene="CGB8" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1346186343" polyA_site 887 /gene="CGB8" /note="major polyA site" variation 887 /gene="CGB8" /replace="a" /replace="g" /db_xref="dbSNP:757000756" ORIGIN
gcttcagtccagcacctttctcgggtcacggcctcctcctggctcccaggaccccaccataggcagaggcaggccttcctacaccctactccctgtgcctccaggctcgactagtccctagcactcgacgactgagtctctgaggtcacttcaccgtggtctccgcctcacccttggcgctggaccagtgagaggagagggctggggcgctccgctgagccactcctgcgcccccctggccttgtctacctcttgccccccgaagggttagtgtcgagctcactccagcatcctacaacctcctggtggccttgccgcccccacaaccccgaggtttaaagccaggtacacgaggcaggggacacaccaaggatggagatgttccaggggctgctgctgttgctgctgctgagcatgggcgggacatgggcatccaaggagccgcttcggccacggtgccgccccatcaatgccaccctggctgtggagaaggagggctgccccgtgtgcatcaccgtcaacaccaccatctgtgccggctactgccccaccatgacccgcgtgctgcagggggtcctgccggccctgcctcaggtggtgtgcaactaccgcgatgtgcgcttcgagtccatccggctccctggctgcccgcgcggcgtgaaccccgtggtctcctacgccgtggctctcagctgtcaatgtgcactctgccgccgcagcaccactgactgcgggggtcccaaggaccaccccttgacctgtgatgacccccgcttccaggactcctcttcctcaaaggcccctccccccagccttccaagtccatcccgactcccggggccctcggacaccccgatcctcccacaataaaggcttctcaatccgca
//
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]