Canonical Allele Identifier: CA89679289

Gene: ADIPOQ ADIPOQ-AS1

Linked Data

• dbSNP Id: rs933764141
• gnomAD v3: 3-186856210-G-T
• gnomAD v4: 3-186856210-G-T
• MyVariant Identifiers: chr3:g.186573999G>T (hg19) ; chr3:g.186856210G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186856210G>T , CM000665.2:g.186856210G>T	GRCh38
NC_000003.11:g.186573999G>T , CM000665.1:g.186573999G>T	GRCh37
NC_000003.10:g.188056693G>T	NCBI36
NG_021140.1:g.18537G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000320741.7:c.*1506G>T (ADIPOQ) MANE Select	ENSP00000320709.2:n.*1506G>T
ENST00000320741.6:c.*1506G>T (ADIPOQ)	ENSP00000320709.2:n.*1506G>T
ENST00000444204.2:c.*1506G>T (ADIPOQ)	ENSP00000389814.2:n.*1506G>T
NM_001177800.1:c.*1506G>T (ADIPOQ)	NP_001171271.1:n.*1506G>T
NM_004797.3:c.*1506G>T (ADIPOQ)	NP_004788.1:n.*1506G>T
XM_011513324.1:c.*1506G>T (ADIPOQ)	XP_011511626.1:n.*1506G>T
NR_046662.2:n.137-94C>A (ADIPOQ-AS1)
NM_004797.4:c.*1506G>T (ADIPOQ) MANE Select	NP_004788.1:n.*1506G>T
NM_001177800.2:c.*1506G>T (ADIPOQ)	NP_001171271.1:n.*1506G>T