Canonical Allele Identifier: CA478097011
Gene: ADIPOR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.1889741T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1780575T>A , CM000674.2:g.1780575T>A GRCh38
NC_000012.11:g.1889741T>A , CM000674.1:g.1889741T>A GRCh37
NC_000012.10:g.1760002T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357103.5:c.588T>A MANE Select ENSP00000349616.4:p.Ser196=
ENST00000357103.4:c.588T>A ENSP00000349616.4:p.Ser196=
ENST00000537190.1:n.428T>A
NM_024551.2:c.588T>A NP_078827.2:p.Ser196=
XM_005253789.1:c.588T>A XP_005253846.1:p.Ser196=
XM_006719018.1:c.588T>A XP_006719081.1:p.Ser196=
XM_011521024.1:c.588T>A XP_011519326.1:p.Ser196=
XM_011521025.1:c.463+2550T>A XP_011519327.1:n.463+2550T>A
XM_005253789.2:c.588T>A XP_005253846.1:p.Ser196=
XM_006719018.2:c.588T>A XP_006719081.1:p.Ser196=
XM_011521024.2:c.588T>A XP_011519326.1:p.Ser196=
NM_024551.3:c.588T>A MANE Select NP_078827.2:p.Ser196=
NM_001375363.1:c.588T>A NP_001362292.1:p.Ser196=
NM_001375364.1:c.588T>A NP_001362293.1:p.Ser196=
NM_001375365.1:c.588T>A NP_001362294.1:p.Ser196=