Canonical Allele Identifier: CA1619675186

Gene: HLA-DQB1 HLA-DQB1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32660167A= , CM000668.2:g.32660167A=	GRCh38
NC_000006.11:g.32627944A= , CM000668.1:g.32627944A=	GRCh37
NC_000006.10:g.32735922A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*69T= (HLA-DQB1) MANE Select	ENSP00000407332.2:n.*69T=
ENST00000374943.8:c.*69T= (HLA-DQB1)	ENSP00000364080.4:n.*69T=
ENST00000399079.7:c.*69T= (HLA-DQB1)	ENSP00000382029.3:n.*69T=
ENST00000399082.7:c.*69T= (HLA-DQB1)	ENSP00000382032.3:n.*69T=
ENST00000399084.5:c.*69T= (HLA-DQB1)	ENSP00000382034.1:n.*69T=
ENST00000434651.6:c.*69T= (HLA-DQB1)	ENSP00000407332.2:n.*69T=
ENST00000443574.1:n.98-70T= (HLA-DQB1)
ENST00000460185.1:n.147T= (HLA-DQB1)
ENST00000484729.2:c.*281T= (HLA-DQB1)	ENSP00000436686.1:n.*281T=
ENST00000487676.1:n.3944T= (HLA-DQB1)
NM_001243961.1:c.*69T= (HLA-DQB1)	NP_001230890.1:n.*69T=
NM_002123.4:c.*69T= (HLA-DQB1)	NP_002114.3:n.*69T=
NR_133907.1:n.177+111A= (HLA-DQB1-AS1)
NM_001243961.2:c.*69T= (HLA-DQB1)	NP_001230890.1:n.*69T=
NM_002123.5:c.*69T= (HLA-DQB1) MANE Select	NP_002114.3:n.*69T=