Canonical Allele Identifier: CA3743882

Gene: HLA-DQA1

Linked Data

• dbSNP Id: rs760756426
• ExAC: 6:32609755 C / G
• gnomAD v2: 6-32609755-C-G
• gnomAD v4: 6-32641978-C-G
• MyVariant Identifiers: chr6:g.32609755C>G (hg19) ; chr6:g.32641978C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32641978C>G , CM000668.2:g.32641978C>G	GRCh38
NC_000006.11:g.32609755C>G , CM000668.1:g.32609755C>G	GRCh37
NC_000006.10:g.32717733C>G	NCBI36
NG_032876.1:g.9573C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343139.11:c.338C>G MANE Select	ENSP00000339398.5:p.Pro113Arg
ENST00000343139.9:c.338C>G	ENSP00000339398.5:p.Pro113Arg
ENST00000374949.2:c.338C>G	ENSP00000364087.2:p.Pro113Arg
ENST00000395363.5:c.338C>G	ENSP00000378767.1:p.Pro113Arg
ENST00000460633.1:n.366C>G
ENST00000482745.5:c.*1170C>G	ENSP00000436546.1:n.*1170C>G
ENST00000496318.5:c.338C>G	ENSP00000437302.1:p.Pro113Arg
NM_002122.3:c.338C>G	NP_002113.2:p.Pro113Arg
XM_006715079.2:c.338C>G	XP_006715142.1:p.Pro113Arg
XM_006715079.4:c.338C>G	XP_006715142.1:p.Pro113Arg
XR_001744085.1:n.86+610G>C
NM_002122.5:c.338C>G MANE Select	NP_002113.2:p.Pro113Arg