Canonical Allele Identifier: CA2581064750
Gene: ADIPOR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1787613G>C , CM000674.2:g.1787613G>C GRCh38
NC_000012.11:g.1896779G>C , CM000674.1:g.1896779G>C GRCh37
NC_000012.10:g.1767040G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357103.5:c.*1541G>C MANE Select ENSP00000349616.4:n.*1541G>C
ENST00000357103.4:c.*1541G>C ENSP00000349616.4:n.*1541G>C
NM_024551.2:c.*1541G>C NP_078827.2:n.*1541G>C
XM_005253789.1:c.*1541G>C XP_005253846.1:n.*1541G>C
XM_006719018.1:c.*1541G>C XP_006719081.1:n.*1541G>C
XM_011521024.1:c.*1541G>C XP_011519326.1:n.*1541G>C
XM_011521025.1:c.*1541G>C XP_011519327.1:n.*1541G>C
XM_005253789.2:c.*1541G>C XP_005253846.1:n.*1541G>C
XM_006719018.2:c.*1541G>C XP_006719081.1:n.*1541G>C
XM_011521024.2:c.*1541G>C XP_011519326.1:n.*1541G>C
NM_024551.3:c.*1541G>C MANE Select NP_078827.2:n.*1541G>C
NM_001375363.1:c.*1541G>C NP_001362292.1:n.*1541G>C
NM_001375364.1:c.*1541G>C NP_001362293.1:n.*1541G>C
NM_001375365.1:c.*1541G>C NP_001362294.1:n.*1541G>C