Canonical Allele Identifier: CA449830862
Gene: HLA-DQA1 HGNC NCBI

Linked Data

gnomAD v4: 6-32642006-C-A
MyVariant Identifiers: chr6:g.32609783C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32642006C>A , CM000668.2:g.32642006C>A GRCh38
NC_000006.11:g.32609783C>A , CM000668.1:g.32609783C>A GRCh37
NC_000006.10:g.32717761C>A NCBI36
NG_032876.1:g.9601C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343139.11:c.366C>A MANE Select ENSP00000339398.5:p.Pro122=
ENST00000343139.9:c.366C>A ENSP00000339398.5:p.Pro122=
ENST00000374949.2:c.366C>A ENSP00000364087.2:p.Pro122=
ENST00000395363.5:c.366C>A ENSP00000378767.1:p.Pro122=
ENST00000460633.1:n.394C>A
ENST00000482745.5:c.*1198C>A ENSP00000436546.1:n.*1198C>A
ENST00000496318.5:c.366C>A ENSP00000437302.1:p.Pro122=
NM_002122.3:c.366C>A NP_002113.2:p.Pro122=
XM_006715079.2:c.366C>A XP_006715142.1:p.Pro122=
XM_006715079.4:c.366C>A XP_006715142.1:p.Pro122=
XR_001744085.1:n.86+582G>T
NM_002122.5:c.366C>A MANE Select NP_002113.2:p.Pro122=