Canonical Allele Identifier: CA89669357
Gene: ADIPOQ HGNC NCBI

Linked Data

dbSNP Id: rs1012282840
MyVariant Identifiers: chr3:g.186560657G>C (hg19) chr3:g.186842868G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186842868G>C , CM000665.2:g.186842868G>C GRCh38
NC_000003.11:g.186560657G>C , CM000665.1:g.186560657G>C GRCh37
NC_000003.10:g.188043351G>C NCBI36
NG_021140.1:g.5195G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320741.7:c.-9+119G>C MANE Select ENSP00000320709.2:n.-9+119G>C
ENST00000320741.6:c.-9+119G>C ENSP00000320709.2:n.-9+119G>C
ENST00000444204.2:c.-60+119G>C ENSP00000389814.2:n.-60+119G>C
NM_001177800.1:c.-60+119G>C NP_001171271.1:n.-60+119G>C
NM_004797.3:c.-9+119G>C NP_004788.1:n.-9+119G>C
XM_011513324.1:c.-125+119G>C XP_011511626.1:n.-125+119G>C
NM_004797.4:c.-9+119G>C MANE Select NP_004788.1:n.-9+119G>C
NM_001177800.2:c.-60+119G>C NP_001171271.1:n.-60+119G>C
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