Canonical Allele Identifier: CA449830870
Gene: HLA-DQA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32609786G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32642009G>A , CM000668.2:g.32642009G>A GRCh38
NC_000006.11:g.32609786G>A , CM000668.1:g.32609786G>A GRCh37
NC_000006.10:g.32717764G>A NCBI36
NG_032876.1:g.9604G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.369G>A MANE Select ENSP00000339398.5:p.Val123=
ENST00000343139.9:c.369G>A ENSP00000339398.5:p.Val123=
ENST00000374949.2:c.369G>A ENSP00000364087.2:p.Val123=
ENST00000395363.5:c.369G>A ENSP00000378767.1:p.Val123=
ENST00000460633.1:n.397G>A
ENST00000482745.5:c.*1201G>A ENSP00000436546.1:n.*1201G>A
ENST00000496318.5:c.369G>A ENSP00000437302.1:p.Val123=
NM_002122.3:c.369G>A NP_002113.2:p.Val123=
XM_006715079.2:c.369G>A XP_006715142.1:p.Val123=
XM_006715079.4:c.369G>A XP_006715142.1:p.Val123=
XR_001744085.1:n.86+579C>T
NM_002122.5:c.369G>A MANE Select NP_002113.2:p.Val123=