Canonical Allele Identifier: CA383652321
Gene: ADIPOR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1780606C>T , CM000674.2:g.1780606C>T GRCh38
NC_000012.11:g.1889772C>T , CM000674.1:g.1889772C>T GRCh37
NC_000012.10:g.1760033C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357103.5:c.619C>T MANE Select ENSP00000349616.4:p.His207Tyr
ENST00000357103.4:c.619C>T ENSP00000349616.4:p.His207Tyr
ENST00000537190.1:n.459C>T
NM_024551.2:c.619C>T NP_078827.2:p.His207Tyr
XM_005253789.1:c.619C>T XP_005253846.1:p.His207Tyr
XM_006719018.1:c.619C>T XP_006719081.1:p.His207Tyr
XM_011521024.1:c.619C>T XP_011519326.1:p.His207Tyr
XM_011521025.1:c.463+2581C>T XP_011519327.1:n.463+2581C>T
XM_005253789.2:c.619C>T XP_005253846.1:p.His207Tyr
XM_006719018.2:c.619C>T XP_006719081.1:p.His207Tyr
XM_011521024.2:c.619C>T XP_011519326.1:p.His207Tyr
NM_024551.3:c.619C>T MANE Select NP_078827.2:p.His207Tyr
NM_001375363.1:c.619C>T NP_001362292.1:p.His207Tyr
NM_001375364.1:c.619C>T NP_001362293.1:p.His207Tyr
NM_001375365.1:c.619C>T NP_001362294.1:p.His207Tyr