Canonical Allele Identifier: CA449831167
Gene: HLA-DQA1 HGNC NCBI

Linked Data

gnomAD v4: 6-32642192-T-C
MyVariant Identifiers: chr6:g.32609969T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32642192T>C , CM000668.2:g.32642192T>C GRCh38
NC_000006.11:g.32609969T>C , CM000668.1:g.32609969T>C GRCh37
NC_000006.10:g.32717947T>C NCBI36
NG_032876.1:g.9787T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343139.11:c.552T>C MANE Select ENSP00000339398.5:p.Asp184=
ENST00000343139.9:c.552T>C ENSP00000339398.5:p.Asp184=
ENST00000374949.2:c.552T>C ENSP00000364087.2:p.Asp184=
ENST00000395363.5:c.552T>C ENSP00000378767.1:p.Asp184=
ENST00000460633.1:n.580T>C
ENST00000482745.5:c.*1384T>C ENSP00000436546.1:n.*1384T>C
ENST00000496318.5:c.552T>C ENSP00000437302.1:p.Asp184=
NM_002122.3:c.552T>C NP_002113.2:p.Asp184=
XM_006715079.2:c.552T>C XP_006715142.1:p.Asp184=
XM_006715079.4:c.552T>C XP_006715142.1:p.Asp184=
XR_001744085.1:n.86+396A>G
NM_002122.5:c.552T>C MANE Select NP_002113.2:p.Asp184=