Canonical Allele Identifier: CA383652258
Gene: ADIPOR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1780579T>A , CM000674.2:g.1780579T>A GRCh38
NC_000012.11:g.1889745T>A , CM000674.1:g.1889745T>A GRCh37
NC_000012.10:g.1760006T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357103.5:c.592T>A MANE Select ENSP00000349616.4:p.Ser198Thr
ENST00000357103.4:c.592T>A ENSP00000349616.4:p.Ser198Thr
ENST00000537190.1:n.432T>A
NM_024551.2:c.592T>A NP_078827.2:p.Ser198Thr
XM_005253789.1:c.592T>A XP_005253846.1:p.Ser198Thr
XM_006719018.1:c.592T>A XP_006719081.1:p.Ser198Thr
XM_011521024.1:c.592T>A XP_011519326.1:p.Ser198Thr
XM_011521025.1:c.463+2554T>A XP_011519327.1:n.463+2554T>A
XM_005253789.2:c.592T>A XP_005253846.1:p.Ser198Thr
XM_006719018.2:c.592T>A XP_006719081.1:p.Ser198Thr
XM_011521024.2:c.592T>A XP_011519326.1:p.Ser198Thr
NM_024551.3:c.592T>A MANE Select NP_078827.2:p.Ser198Thr
NM_001375363.1:c.592T>A NP_001362292.1:p.Ser198Thr
NM_001375364.1:c.592T>A NP_001362293.1:p.Ser198Thr
NM_001375365.1:c.592T>A NP_001362294.1:p.Ser198Thr