Canonical Allele Identifier: CA602886022

Gene: ADIPOR2

Linked Data

• gnomAD v2: 12-1837026-A-C
• MyVariant Identifiers: chr12:g.1837026A>C (hg19) ; chr12:g.1727860A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1727860A>C , CM000674.2:g.1727860A>C	GRCh38
NC_000012.11:g.1837026A>C , CM000674.1:g.1837026A>C	GRCh37
NC_000012.10:g.1707287A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.-86-26398A>C MANE Select	ENSP00000349616.4:n.-86-26398A>C
ENST00000357103.4:c.-86-26398A>C	ENSP00000349616.4:n.-86-26398A>C
ENST00000537545.1:n.145-26398A>C
ENST00000540974.1:n.149-2865A>C
NM_024551.2:c.-86-26398A>C	NP_078827.2:n.-86-26398A>C
XM_005253789.1:c.-86-26398A>C	XP_005253846.1:n.-86-26398A>C
XM_006719018.1:c.-87+24878A>C	XP_006719081.1:n.-87+24878A>C
XM_011521024.1:c.-87+24878A>C	XP_011519326.1:n.-87+24878A>C
XM_011521025.1:c.-86-26398A>C	XP_011519327.1:n.-86-26398A>C
XM_005253789.2:c.-86-26398A>C	XP_005253846.1:n.-86-26398A>C
XM_006719018.2:c.-87+24878A>C	XP_006719081.1:n.-87+24878A>C
XM_011521024.2:c.-87+24878A>C	XP_011519326.1:n.-87+24878A>C
NM_024551.3:c.-86-26398A>C MANE Select	NP_078827.2:n.-86-26398A>C
NM_001375363.1:c.-86-26398A>C	NP_001362292.1:n.-86-26398A>C
NM_001375364.1:c.-248-8219A>C	NP_001362293.1:n.-248-8219A>C
NM_001375365.1:c.-86-26398A>C	NP_001362294.1:n.-86-26398A>C