Canonical Allele Identifier: CA117161
Gene: ADIPOQ HGNC NCBI
ADIPOQ-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4990
ClinVar RCV Id: RCV003227598
dbSNP Id: rs121917815
ExAC: 3:186572092 C / T
gnomAD v2: 3-186572092-C-T
gnomAD v4: 3-186854303-C-T
MyVariant Identifiers: chr3:g.186572092C>T (hg19) chr3:g.186854303C>T (hg38)
PubMed: PMID:10918532 PMID:12878598
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186854303C>T , CM000665.2:g.186854303C>T GRCh38
NC_000003.11:g.186572092C>T , CM000665.1:g.186572092C>T GRCh37
NC_000003.10:g.188054786C>T NCBI36
NG_021140.1:g.16630C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320741.7:c.334C>T (ADIPOQ) MANE Select ENSP00000320709.2:p.Arg112Cys
ENST00000320741.6:c.334C>T (ADIPOQ) ENSP00000320709.2:p.Arg112Cys
ENST00000444204.2:c.334C>T (ADIPOQ) ENSP00000389814.2:p.Arg112Cys
NM_001177800.1:c.334C>T (ADIPOQ) NP_001171271.1:p.Arg112Cys
NM_004797.3:c.334C>T (ADIPOQ) NP_004788.1:p.Arg112Cys
NR_046662.1:n.1821G>A (ADIPOQ-AS1)
XM_011513324.1:c.334C>T (ADIPOQ) XP_011511626.1:p.Arg112Cys
NR_046662.2:n.1950G>A (ADIPOQ-AS1)
NM_004797.4:c.334C>T (ADIPOQ) MANE Select NP_004788.1:p.Arg112Cys
NM_001177800.2:c.334C>T (ADIPOQ) NP_001171271.1:p.Arg112Cys
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