Canonical Allele Identifier: CA449830972

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs1048173
• gnomAD v2: 6-32609855-A-T
• gnomAD v4: 6-32642078-A-T
• MyVariant Identifiers: chr6:g.32609855A>T (hg19) ; chr6:g.32642078A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32642078A>T , CM000668.2:g.32642078A>T	GRCh38
NC_000006.11:g.32609855A>T , CM000668.1:g.32609855A>T	GRCh37
NC_000006.10:g.32717833A>T	NCBI36
NG_032876.1:g.9673A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.438A>T MANE Select	ENSP00000339398.5:p.Thr146=
ENST00000343139.9:c.438A>T	ENSP00000339398.5:p.Thr146=
ENST00000374949.2:c.438A>T	ENSP00000364087.2:p.Thr146=
ENST00000395363.5:c.438A>T	ENSP00000378767.1:p.Thr146=
ENST00000460633.1:n.466A>T
ENST00000482745.5:c.*1270A>T	ENSP00000436546.1:n.*1270A>T
ENST00000496318.5:c.438A>T	ENSP00000437302.1:p.Thr146=
NM_002122.3:c.438A>T	NP_002113.2:p.Thr146=
XM_006715079.2:c.438A>T	XP_006715142.1:p.Thr146=
XM_006715079.4:c.438A>T	XP_006715142.1:p.Thr146=
XR_001744085.1:n.86+510T>A
NM_002122.5:c.438A>T MANE Select	NP_002113.2:p.Thr146=