Canonical Allele Identifier: CA2678168081
Gene: HLA-DQA1 HGNC NCBI

Linked Data

gnomAD v4: 6-32641651-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32641651A>C , CM000668.2:g.32641651A>C GRCh38
NC_000006.11:g.32609428A>C , CM000668.1:g.32609428A>C GRCh37
NC_000006.10:g.32717406A>C NCBI36
NG_032876.1:g.9246A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.331+93A>C MANE Select ENSP00000339398.5:n.331+93A>C
ENST00000343139.9:c.331+93A>C ENSP00000339398.5:n.331+93A>C
ENST00000374949.2:c.331+93A>C ENSP00000364087.2:n.331+93A>C
ENST00000395363.5:c.331+93A>C ENSP00000378767.1:n.331+93A>C
ENST00000460633.1:n.359+93A>C
ENST00000482745.5:c.*1163+93A>C ENSP00000436546.1:n.*1163+93A>C
ENST00000496318.5:c.331+93A>C ENSP00000437302.1:n.331+93A>C
NM_002122.3:c.331+93A>C NP_002113.2:n.331+93A>C
XM_006715079.2:c.331+93A>C XP_006715142.1:n.331+93A>C
XM_006715079.4:c.331+93A>C XP_006715142.1:n.331+93A>C
XR_001744085.1:n.86+937T>G
NM_002122.5:c.331+93A>C MANE Select NP_002113.2:n.331+93A>C