Canonical Allele Identifier: CA602896447

Gene: ADIPOR2

Linked Data

• dbSNP Id: rs1214436192
• gnomAD v2: 12-1896984-G-A
• gnomAD v3: 12-1787818-G-A
• gnomAD v4: 12-1787818-G-A
• MyVariant Identifiers: chr12:g.1896984G>A (hg19) ; chr12:g.1787818G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1787818G>A , CM000674.2:g.1787818G>A	GRCh38
NC_000012.11:g.1896984G>A , CM000674.1:g.1896984G>A	GRCh37
NC_000012.10:g.1767245G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.*1746G>A MANE Select	ENSP00000349616.4:n.*1746G>A
ENST00000357103.4:c.*1746G>A	ENSP00000349616.4:n.*1746G>A
NM_024551.2:c.*1746G>A	NP_078827.2:n.*1746G>A
XM_005253789.1:c.*1746G>A	XP_005253846.1:n.*1746G>A
XM_006719018.1:c.*1746G>A	XP_006719081.1:n.*1746G>A
XM_011521024.1:c.*1746G>A	XP_011519326.1:n.*1746G>A
XM_011521025.1:c.*1746G>A	XP_011519327.1:n.*1746G>A
XM_005253789.2:c.*1746G>A	XP_005253846.1:n.*1746G>A
XM_006719018.2:c.*1746G>A	XP_006719081.1:n.*1746G>A
XM_011521024.2:c.*1746G>A	XP_011519326.1:n.*1746G>A
NM_024551.3:c.*1746G>A MANE Select	NP_078827.2:n.*1746G>A
NM_001375363.1:c.*1746G>A	NP_001362292.1:n.*1746G>A
NM_001375364.1:c.*1746G>A	NP_001362293.1:n.*1746G>A
NM_001375365.1:c.*1746G>A	NP_001362294.1:n.*1746G>A