Canonical Allele Identifier: CA2012145305
Gene: ADIPOR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1787854G= , CM000674.2:g.1787854G= GRCh38
NC_000012.11:g.1897020G= , CM000674.1:g.1897020G= GRCh37
NC_000012.10:g.1767281G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357103.5:c.*1782G= MANE Select ENSP00000349616.4:n.*1782G=
ENST00000357103.4:c.*1782G= ENSP00000349616.4:n.*1782G=
NM_024551.2:c.*1782G= NP_078827.2:n.*1782G=
XM_005253789.1:c.*1782G= XP_005253846.1:n.*1782G=
XM_006719018.1:c.*1782G= XP_006719081.1:n.*1782G=
XM_011521024.1:c.*1782G= XP_011519326.1:n.*1782G=
XM_011521025.1:c.*1782G= XP_011519327.1:n.*1782G=
XM_005253789.2:c.*1782G= XP_005253846.1:n.*1782G=
XM_006719018.2:c.*1782G= XP_006719081.1:n.*1782G=
XM_011521024.2:c.*1782G= XP_011519326.1:n.*1782G=
NM_024551.3:c.*1782G= MANE Select NP_078827.2:n.*1782G=
NM_001375363.1:c.*1782G= NP_001362292.1:n.*1782G=
NM_001375364.1:c.*1782G= NP_001362293.1:n.*1782G=
NM_001375365.1:c.*1782G= NP_001362294.1:n.*1782G=