Canonical Allele Identifier: CA6385798

Gene: ADIPOR2

Linked Data

• dbSNP Id: rs768568170
• ExAC: 12:1890121 C / T
• gnomAD v2: 12-1890121-C-T
• MyVariant Identifiers: chr12:g.1890121C>T (hg19) ; chr12:g.1780955C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780955C>T , CM000674.2:g.1780955C>T	GRCh38
NC_000012.11:g.1890121C>T , CM000674.1:g.1890121C>T	GRCh37
NC_000012.10:g.1760382C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357103.5:c.717C>T MANE Select	ENSP00000349616.4:p.Phe239=
ENST00000357103.4:c.717C>T	ENSP00000349616.4:p.Phe239=
ENST00000537190.1:n.557C>T
NM_024551.2:c.717C>T	NP_078827.2:p.Phe239=
XM_005253789.1:c.717C>T	XP_005253846.1:p.Phe239=
XM_006719018.1:c.717C>T	XP_006719081.1:p.Phe239=
XM_011521024.1:c.717C>T	XP_011519326.1:p.Phe239=
XM_011521025.1:c.464-2925C>T	XP_011519327.1:n.464-2925C>T
XM_005253789.2:c.717C>T	XP_005253846.1:p.Phe239=
XM_006719018.2:c.717C>T	XP_006719081.1:p.Phe239=
XM_011521024.2:c.717C>T	XP_011519326.1:p.Phe239=
NM_024551.3:c.717C>T MANE Select	NP_078827.2:p.Phe239=
NM_001375363.1:c.717C>T	NP_001362292.1:p.Phe239=
NM_001375364.1:c.717C>T	NP_001362293.1:p.Phe239=
NM_001375365.1:c.717C>T	NP_001362294.1:p.Phe239=