Canonical Allele Identifier: CA383652272

Gene: ADIPOR2

Linked Data

• gnomAD v4: 12-1780585-C-G
• MyVariant Identifiers: chr12:g.1889751C>G (hg19) ; chr12:g.1780585C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780585C>G , CM000674.2:g.1780585C>G	GRCh38
NC_000012.11:g.1889751C>G , CM000674.1:g.1889751C>G	GRCh37
NC_000012.10:g.1760012C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.598C>G MANE Select	ENSP00000349616.4:p.Leu200Val
ENST00000357103.4:c.598C>G	ENSP00000349616.4:p.Leu200Val
ENST00000537190.1:n.438C>G
NM_024551.2:c.598C>G	NP_078827.2:p.Leu200Val
XM_005253789.1:c.598C>G	XP_005253846.1:p.Leu200Val
XM_006719018.1:c.598C>G	XP_006719081.1:p.Leu200Val
XM_011521024.1:c.598C>G	XP_011519326.1:p.Leu200Val
XM_011521025.1:c.463+2560C>G	XP_011519327.1:n.463+2560C>G
XM_005253789.2:c.598C>G	XP_005253846.1:p.Leu200Val
XM_006719018.2:c.598C>G	XP_006719081.1:p.Leu200Val
XM_011521024.2:c.598C>G	XP_011519326.1:p.Leu200Val
NM_024551.3:c.598C>G MANE Select	NP_078827.2:p.Leu200Val
NM_001375363.1:c.598C>G	NP_001362292.1:p.Leu200Val
NM_001375364.1:c.598C>G	NP_001362293.1:p.Leu200Val
NM_001375365.1:c.598C>G	NP_001362294.1:p.Leu200Val