Canonical Allele Identifier: CA2012138850

Gene: ADIPOR2

Linked Data

• dbSNP Id: rs1565659151
• gnomAD v4: 12-1780412-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780412G>C , CM000674.2:g.1780412G>C	GRCh38
NC_000012.11:g.1889578G>C , CM000674.1:g.1889578G>C	GRCh37
NC_000012.10:g.1759839G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.464-39G>C MANE Select	ENSP00000349616.4:n.464-39G>C
ENST00000357103.4:c.464-39G>C	ENSP00000349616.4:n.464-39G>C
ENST00000535774.1:n.421-39G>C
ENST00000537190.1:n.265G>C
NM_024551.2:c.464-39G>C	NP_078827.2:n.464-39G>C
XM_005253789.1:c.464-39G>C	XP_005253846.1:n.464-39G>C
XM_006719018.1:c.464-39G>C	XP_006719081.1:n.464-39G>C
XM_011521024.1:c.464-39G>C	XP_011519326.1:n.464-39G>C
XM_011521025.1:c.463+2387G>C	XP_011519327.1:n.463+2387G>C
XM_005253789.2:c.464-39G>C	XP_005253846.1:n.464-39G>C
XM_006719018.2:c.464-39G>C	XP_006719081.1:n.464-39G>C
XM_011521024.2:c.464-39G>C	XP_011519326.1:n.464-39G>C
NM_024551.3:c.464-39G>C MANE Select	NP_078827.2:n.464-39G>C
NM_001375363.1:c.464-39G>C	NP_001362292.1:n.464-39G>C
NM_001375364.1:c.464-39G>C	NP_001362293.1:n.464-39G>C
NM_001375365.1:c.464-39G>C	NP_001362294.1:n.464-39G>C