Canonical Allele Identifier: CA137008333

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs28383457
• gnomAD v2: 6-32609456-C-T
• gnomAD v3: 6-32641679-C-T
• gnomAD v4: 6-32641679-C-T
• MyVariant Identifiers: chr6:g.32609456C>T (hg19) ; chr6:g.32641679C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641679C>T , CM000668.2:g.32641679C>T	GRCh38
NC_000006.11:g.32609456C>T , CM000668.1:g.32609456C>T	GRCh37
NC_000006.10:g.32717434C>T	NCBI36
NG_032876.1:g.9274C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.331+121C>T MANE Select	ENSP00000339398.5:n.331+121C>T
ENST00000343139.9:c.331+121C>T	ENSP00000339398.5:n.331+121C>T
ENST00000374949.2:c.331+121C>T	ENSP00000364087.2:n.331+121C>T
ENST00000395363.5:c.331+121C>T	ENSP00000378767.1:n.331+121C>T
ENST00000460633.1:n.359+121C>T
ENST00000482745.5:c.*1163+121C>T	ENSP00000436546.1:n.*1163+121C>T
ENST00000496318.5:c.331+121C>T	ENSP00000437302.1:n.331+121C>T
NM_002122.3:c.331+121C>T	NP_002113.2:n.331+121C>T
XM_006715079.2:c.331+121C>T	XP_006715142.1:n.331+121C>T
XM_006715079.4:c.331+121C>T	XP_006715142.1:n.331+121C>T
XR_001744085.1:n.86+909G>A
NM_002122.5:c.331+121C>T MANE Select	NP_002113.2:n.331+121C>T