Canonical Allele Identifier: CA478096949

Gene: ADIPOR2

Linked Data

• gnomAD v4: 12-1780476-G-C
• MyVariant Identifiers: chr12:g.1889642G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780476G>C , CM000674.2:g.1780476G>C	GRCh38
NC_000012.11:g.1889642G>C , CM000674.1:g.1889642G>C	GRCh37
NC_000012.10:g.1759903G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.489G>C MANE Select	ENSP00000349616.4:p.Gly163=
ENST00000357103.4:c.489G>C	ENSP00000349616.4:p.Gly163=
ENST00000535774.1:n.446G>C
ENST00000537190.1:n.329G>C
NM_024551.2:c.489G>C	NP_078827.2:p.Gly163=
XM_005253789.1:c.489G>C	XP_005253846.1:p.Gly163=
XM_006719018.1:c.489G>C	XP_006719081.1:p.Gly163=
XM_011521024.1:c.489G>C	XP_011519326.1:p.Gly163=
XM_011521025.1:c.463+2451G>C	XP_011519327.1:n.463+2451G>C
XM_005253789.2:c.489G>C	XP_005253846.1:p.Gly163=
XM_006719018.2:c.489G>C	XP_006719081.1:p.Gly163=
XM_011521024.2:c.489G>C	XP_011519326.1:p.Gly163=
NM_024551.3:c.489G>C MANE Select	NP_078827.2:p.Gly163=
NM_001375363.1:c.489G>C	NP_001362292.1:p.Gly163=
NM_001375364.1:c.489G>C	NP_001362293.1:p.Gly163=
NM_001375365.1:c.489G>C	NP_001362294.1:p.Gly163=