Canonical Allele Identifier: CA823967433

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs1320412832
• gnomAD v3: 6-32641876-G-T
• gnomAD v4: 6-32641876-G-T
• MyVariant Identifiers: chr6:g.32609653G>T (hg19) ; chr6:g.32641876G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641876G>T , CM000668.2:g.32641876G>T	GRCh38
NC_000006.11:g.32609653G>T , CM000668.1:g.32609653G>T	GRCh37
NC_000006.10:g.32717631G>T	NCBI36
NG_032876.1:g.9471G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.332-96G>T MANE Select	ENSP00000339398.5:n.332-96G>T
ENST00000343139.9:c.332-96G>T	ENSP00000339398.5:n.332-96G>T
ENST00000374949.2:c.332-96G>T	ENSP00000364087.2:n.332-96G>T
ENST00000395363.5:c.332-96G>T	ENSP00000378767.1:n.332-96G>T
ENST00000460633.1:n.360-96G>T
ENST00000482745.5:c.*1164-96G>T	ENSP00000436546.1:n.*1164-96G>T
ENST00000496318.5:c.332-96G>T	ENSP00000437302.1:n.332-96G>T
NM_002122.3:c.332-96G>T	NP_002113.2:n.332-96G>T
XM_006715079.2:c.332-96G>T	XP_006715142.1:n.332-96G>T
XM_006715079.4:c.332-96G>T	XP_006715142.1:n.332-96G>T
XR_001744085.1:n.86+712C>A
NM_002122.5:c.332-96G>T MANE Select	NP_002113.2:n.332-96G>T