Canonical Allele Identifier: CA686019974

Gene: ADIPOR2

Linked Data

• dbSNP Id: rs1216964608
• MyVariant Identifiers: chr12:g.1856937C>G (hg19) ; chr12:g.1747771C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1747771C>G , CM000674.2:g.1747771C>G	GRCh38
NC_000012.11:g.1856937C>G , CM000674.1:g.1856937C>G	GRCh37
NC_000012.10:g.1727198C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.-86-6487C>G MANE Select	ENSP00000349616.4:n.-86-6487C>G
ENST00000357103.4:c.-86-6487C>G	ENSP00000349616.4:n.-86-6487C>G
ENST00000537545.1:n.145-6487C>G
NM_024551.2:c.-86-6487C>G	NP_078827.2:n.-86-6487C>G
XM_005253789.1:c.-86-6487C>G	XP_005253846.1:n.-86-6487C>G
XM_006719018.1:c.-86-6487C>G	XP_006719081.1:n.-86-6487C>G
XM_011521024.1:c.-86-6487C>G	XP_011519326.1:n.-86-6487C>G
XM_011521025.1:c.-86-6487C>G	XP_011519327.1:n.-86-6487C>G
XM_005253789.2:c.-86-6487C>G	XP_005253846.1:n.-86-6487C>G
XM_006719018.2:c.-86-6487C>G	XP_006719081.1:n.-86-6487C>G
XM_011521024.2:c.-86-6487C>G	XP_011519326.1:n.-86-6487C>G
NM_024551.3:c.-86-6487C>G MANE Select	NP_078827.2:n.-86-6487C>G
NM_001375363.1:c.-86-6487C>G	NP_001362292.1:n.-86-6487C>G
NM_001375364.1:c.-86-6487C>G	NP_001362293.1:n.-86-6487C>G
NM_001375365.1:c.-86-6487C>G	NP_001362294.1:n.-86-6487C>G