Canonical Allele Identifier: CA383652050
Gene: ADIPOR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1780487T>C , CM000674.2:g.1780487T>C GRCh38
NC_000012.11:g.1889653T>C , CM000674.1:g.1889653T>C GRCh37
NC_000012.10:g.1759914T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357103.5:c.500T>C MANE Select ENSP00000349616.4:p.Met167Thr
ENST00000357103.4:c.500T>C ENSP00000349616.4:p.Met167Thr
ENST00000535774.1:n.457T>C
ENST00000537190.1:n.340T>C
NM_024551.2:c.500T>C NP_078827.2:p.Met167Thr
XM_005253789.1:c.500T>C XP_005253846.1:p.Met167Thr
XM_006719018.1:c.500T>C XP_006719081.1:p.Met167Thr
XM_011521024.1:c.500T>C XP_011519326.1:p.Met167Thr
XM_011521025.1:c.463+2462T>C XP_011519327.1:n.463+2462T>C
XM_005253789.2:c.500T>C XP_005253846.1:p.Met167Thr
XM_006719018.2:c.500T>C XP_006719081.1:p.Met167Thr
XM_011521024.2:c.500T>C XP_011519326.1:p.Met167Thr
NM_024551.3:c.500T>C MANE Select NP_078827.2:p.Met167Thr
NM_001375363.1:c.500T>C NP_001362292.1:p.Met167Thr
NM_001375364.1:c.500T>C NP_001362293.1:p.Met167Thr
NM_001375365.1:c.500T>C NP_001362294.1:p.Met167Thr