Canonical Allele Identifier: CA231905342

Gene: ADIPOR2

Linked Data

• dbSNP Id: rs200439501
• gnomAD v2: 12-1889919-T-A
• gnomAD v3: 12-1780753-T-A
• gnomAD v4: 12-1780753-T-A
• MyVariant Identifiers: chr12:g.1889919T>A (hg19) ; chr12:g.1780753T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780753T>A , CM000674.2:g.1780753T>A	GRCh38
NC_000012.11:g.1889919T>A , CM000674.1:g.1889919T>A	GRCh37
NC_000012.10:g.1760180T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.650+116T>A MANE Select	ENSP00000349616.4:n.650+116T>A
ENST00000357103.4:c.650+116T>A	ENSP00000349616.4:n.650+116T>A
ENST00000537190.1:n.490+116T>A
NM_024551.2:c.650+116T>A	NP_078827.2:n.650+116T>A
XM_005253789.1:c.650+116T>A	XP_005253846.1:n.650+116T>A
XM_006719018.1:c.650+116T>A	XP_006719081.1:n.650+116T>A
XM_011521024.1:c.650+116T>A	XP_011519326.1:n.650+116T>A
XM_011521025.1:c.463+2728T>A	XP_011519327.1:n.463+2728T>A
XM_005253789.2:c.650+116T>A	XP_005253846.1:n.650+116T>A
XM_006719018.2:c.650+116T>A	XP_006719081.1:n.650+116T>A
XM_011521024.2:c.650+116T>A	XP_011519326.1:n.650+116T>A
NM_024551.3:c.650+116T>A MANE Select	NP_078827.2:n.650+116T>A
NM_001375363.1:c.650+116T>A	NP_001362292.1:n.650+116T>A
NM_001375364.1:c.650+116T>A	NP_001362293.1:n.650+116T>A
NM_001375365.1:c.650+116T>A	NP_001362294.1:n.650+116T>A