Canonical Allele Identifier: CA383651971

Gene: ADIPOR2

Linked Data

• gnomAD v3: 12-1780451-G-T
• gnomAD v4: 12-1780451-G-T
• MyVariant Identifiers: chr12:g.1889617G>T (hg19) ; chr12:g.1780451G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780451G>T , CM000674.2:g.1780451G>T	GRCh38
NC_000012.11:g.1889617G>T , CM000674.1:g.1889617G>T	GRCh37
NC_000012.10:g.1759878G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.464G>T MANE Select	ENSP00000349616.4:p.Gly155Val
ENST00000357103.4:c.464G>T	ENSP00000349616.4:p.Gly155Val
ENST00000535774.1:n.421G>T
ENST00000537190.1:n.304G>T
NM_024551.2:c.464G>T	NP_078827.2:p.Gly155Val
XM_005253789.1:c.464G>T	XP_005253846.1:p.Gly155Val
XM_006719018.1:c.464G>T	XP_006719081.1:p.Gly155Val
XM_011521024.1:c.464G>T	XP_011519326.1:p.Gly155Val
XM_011521025.1:c.463+2426G>T	XP_011519327.1:n.463+2426G>T
XM_005253789.2:c.464G>T	XP_005253846.1:p.Gly155Val
XM_006719018.2:c.464G>T	XP_006719081.1:p.Gly155Val
XM_011521024.2:c.464G>T	XP_011519326.1:p.Gly155Val
NM_024551.3:c.464G>T MANE Select	NP_078827.2:p.Gly155Val
NM_001375363.1:c.464G>T	NP_001362292.1:p.Gly155Val
NM_001375364.1:c.464G>T	NP_001362293.1:p.Gly155Val
NM_001375365.1:c.464G>T	NP_001362294.1:p.Gly155Val