Canonical Allele Identifier: CA6385747

Gene: ADIPOR2

Linked Data

• dbSNP Id: rs747342627
• ExAC: 12:1889584 T / C
• gnomAD v2: 12-1889584-T-C
• gnomAD v4: 12-1780418-T-C
• MyVariant Identifiers: chr12:g.1889584T>C (hg19) ; chr12:g.1780418T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780418T>C , CM000674.2:g.1780418T>C	GRCh38
NC_000012.11:g.1889584T>C , CM000674.1:g.1889584T>C	GRCh37
NC_000012.10:g.1759845T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.464-33T>C MANE Select	ENSP00000349616.4:n.464-33T>C
ENST00000357103.4:c.464-33T>C	ENSP00000349616.4:n.464-33T>C
ENST00000535774.1:n.421-33T>C
ENST00000537190.1:n.271T>C
NM_024551.2:c.464-33T>C	NP_078827.2:n.464-33T>C
XM_005253789.1:c.464-33T>C	XP_005253846.1:n.464-33T>C
XM_006719018.1:c.464-33T>C	XP_006719081.1:n.464-33T>C
XM_011521024.1:c.464-33T>C	XP_011519326.1:n.464-33T>C
XM_011521025.1:c.463+2393T>C	XP_011519327.1:n.463+2393T>C
XM_005253789.2:c.464-33T>C	XP_005253846.1:n.464-33T>C
XM_006719018.2:c.464-33T>C	XP_006719081.1:n.464-33T>C
XM_011521024.2:c.464-33T>C	XP_011519326.1:n.464-33T>C
NM_024551.3:c.464-33T>C MANE Select	NP_078827.2:n.464-33T>C
NM_001375363.1:c.464-33T>C	NP_001362292.1:n.464-33T>C
NM_001375364.1:c.464-33T>C	NP_001362293.1:n.464-33T>C
NM_001375365.1:c.464-33T>C	NP_001362294.1:n.464-33T>C