Canonical Allele Identifier: CA2747967

Gene: ADIPOQ ADIPOQ-AS1

Linked Data

• dbSNP Id: rs370574236
• ExAC: 3:186572048 T / C
• gnomAD v2: 3-186572048-T-C
• gnomAD v3: 3-186854259-T-C
• gnomAD v4: 3-186854259-T-C
• MyVariant Identifiers: chr3:g.186572048T>C (hg19) ; chr3:g.186854259T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186854259T>C , CM000665.2:g.186854259T>C	GRCh38
NC_000003.11:g.186572048T>C , CM000665.1:g.186572048T>C	GRCh37
NC_000003.10:g.188054742T>C	NCBI36
NG_021140.1:g.16586T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320741.7:c.290T>C (ADIPOQ) MANE Select	ENSP00000320709.2:p.Ile97Thr
ENST00000320741.6:c.290T>C (ADIPOQ)	ENSP00000320709.2:p.Ile97Thr
ENST00000444204.2:c.290T>C (ADIPOQ)	ENSP00000389814.2:p.Ile97Thr
NM_001177800.1:c.290T>C (ADIPOQ)	NP_001171271.1:p.Ile97Thr
NM_004797.3:c.290T>C (ADIPOQ)	NP_004788.1:p.Ile97Thr
NR_046662.1:n.1865A>G (ADIPOQ-AS1)
XM_011513324.1:c.290T>C (ADIPOQ)	XP_011511626.1:p.Ile97Thr
NR_046662.2:n.1994A>G (ADIPOQ-AS1)
NM_004797.4:c.290T>C (ADIPOQ) MANE Select	NP_004788.1:p.Ile97Thr
NM_001177800.2:c.290T>C (ADIPOQ)	NP_001171271.1:p.Ile97Thr