Canonical Allele Identifier: CA363893991

Gene: HLA-DQB1

Linked Data

• gnomAD v4: 6-32665052-T-A
• MyVariant Identifiers: chr6:g.32632829T>A (hg19) ; chr6:g.32665052T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32665052T>A , CM000668.2:g.32665052T>A	GRCh38
NC_000006.11:g.32632829T>A , CM000668.1:g.32632829T>A	GRCh37
NC_000006.10:g.32740807T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000434651.7:c.125A>T MANE Select	ENSP00000407332.2:p.Gln42Leu
ENST00000374943.8:c.125A>T	ENSP00000364080.4:p.Gln42Leu
ENST00000399079.7:c.125A>T	ENSP00000382029.3:p.Gln42Leu
ENST00000399082.7:c.109+1447A>T	ENSP00000382032.3:n.109+1447A>T
ENST00000399084.5:c.125A>T	ENSP00000382034.1:p.Gln42Leu
ENST00000434651.6:c.125A>T	ENSP00000407332.2:p.Gln42Leu
ENST00000484729.2:c.125A>T	ENSP00000436686.1:p.Gln42Leu
ENST00000487676.1:n.156A>T
NM_001243961.1:c.125A>T	NP_001230890.1:p.Gln42Leu
NM_002123.4:c.125A>T	NP_002114.3:p.Gln42Leu
NM_001243961.2:c.125A>T	NP_001230890.1:p.Gln42Leu
NM_002123.5:c.125A>T MANE Select	NP_002114.3:p.Gln42Leu