Canonical Allele Identifier: CA11430819

Gene: ADIPOQ ADIPOQ-AS1

Linked Data

• dbSNP Id: rs1063539
• gnomAD v2: 3-186575392-G-C
• gnomAD v3: 3-186857603-G-C
• gnomAD v4: 3-186857603-G-C
• MyVariant Identifiers: chr3:g.186575392G>C (hg19) ; chr3:g.186857603G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186857603G>C , CM000665.2:g.186857603G>C	GRCh38
NC_000003.11:g.186575392G>C , CM000665.1:g.186575392G>C	GRCh37
NC_000003.10:g.188058086G>C	NCBI36
NG_021140.1:g.19930G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000320741.7:c.*2899G>C (ADIPOQ) MANE Select	ENSP00000320709.2:n.*2899G>C
ENST00000320741.6:c.*2899G>C (ADIPOQ)	ENSP00000320709.2:n.*2899G>C
ENST00000444204.2:c.*2899G>C (ADIPOQ)	ENSP00000389814.2:n.*2899G>C
NM_001177800.1:c.*2899G>C (ADIPOQ)	NP_001171271.1:n.*2899G>C
NM_004797.3:c.*2899G>C (ADIPOQ)	NP_004788.1:n.*2899G>C
XM_011513324.1:c.*2899G>C (ADIPOQ)	XP_011511626.1:n.*2899G>C
NR_046662.2:n.137-1487C>G (ADIPOQ-AS1)
NM_004797.4:c.*2899G>C (ADIPOQ) MANE Select	NP_004788.1:n.*2899G>C
NM_001177800.2:c.*2899G>C (ADIPOQ)	NP_001171271.1:n.*2899G>C