Canonical Allele Identifier: CA137008457

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs997391246
• gnomAD v3: 6-32641800-G-A
• gnomAD v4: 6-32641800-G-A
• MyVariant Identifiers: chr6:g.32609577G>A (hg19) ; chr6:g.32641800G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641800G>A , CM000668.2:g.32641800G>A	GRCh38
NC_000006.11:g.32609577G>A , CM000668.1:g.32609577G>A	GRCh37
NC_000006.10:g.32717555G>A	NCBI36
NG_032876.1:g.9395G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.332-172G>A MANE Select	ENSP00000339398.5:n.332-172G>A
ENST00000343139.9:c.332-172G>A	ENSP00000339398.5:n.332-172G>A
ENST00000374949.2:c.332-172G>A	ENSP00000364087.2:n.332-172G>A
ENST00000395363.5:c.332-172G>A	ENSP00000378767.1:n.332-172G>A
ENST00000460633.1:n.360-172G>A
ENST00000482745.5:c.*1164-172G>A	ENSP00000436546.1:n.*1164-172G>A
ENST00000496318.5:c.332-172G>A	ENSP00000437302.1:n.332-172G>A
NM_002122.3:c.332-172G>A	NP_002113.2:n.332-172G>A
XM_006715079.2:c.332-172G>A	XP_006715142.1:n.332-172G>A
XM_006715079.4:c.332-172G>A	XP_006715142.1:n.332-172G>A
XR_001744085.1:n.86+788C>T
NM_002122.5:c.332-172G>A MANE Select	NP_002113.2:n.332-172G>A