Canonical Allele Identifier: CA944032816
Gene: ADIPOR2 HGNC NCBI

Linked Data

dbSNP Id: rs952678931
gnomAD v3: 12-1787651-C-G
gnomAD v4: 12-1787651-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1787651C>G , CM000674.2:g.1787651C>G GRCh38
NC_000012.11:g.1896817C>G , CM000674.1:g.1896817C>G GRCh37
NC_000012.10:g.1767078C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357103.5:c.*1579C>G MANE Select ENSP00000349616.4:n.*1579C>G
ENST00000357103.4:c.*1579C>G ENSP00000349616.4:n.*1579C>G
NM_024551.2:c.*1579C>G NP_078827.2:n.*1579C>G
XM_005253789.1:c.*1579C>G XP_005253846.1:n.*1579C>G
XM_006719018.1:c.*1579C>G XP_006719081.1:n.*1579C>G
XM_011521024.1:c.*1579C>G XP_011519326.1:n.*1579C>G
XM_011521025.1:c.*1579C>G XP_011519327.1:n.*1579C>G
XM_005253789.2:c.*1579C>G XP_005253846.1:n.*1579C>G
XM_006719018.2:c.*1579C>G XP_006719081.1:n.*1579C>G
XM_011521024.2:c.*1579C>G XP_011519326.1:n.*1579C>G
NM_024551.3:c.*1579C>G MANE Select NP_078827.2:n.*1579C>G
NM_001375363.1:c.*1579C>G NP_001362292.1:n.*1579C>G
NM_001375364.1:c.*1579C>G NP_001362293.1:n.*1579C>G
NM_001375365.1:c.*1579C>G NP_001362294.1:n.*1579C>G