Canonical Allele Identifier: CA2678151522

Gene: HLA-DQB1

Linked Data

• gnomAD v4: 6-32659742-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659743_32659744dup , CM000668.2:g.32659743_32659744dup	GRCh38
NC_000006.11:g.32627520_32627521dup , CM000668.1:g.32627520_32627521dup	GRCh37
NC_000006.10:g.32735498_32735499dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*492_*493dup MANE Select	ENSP00000407332.2:n.*492_*493dup
ENST00000374943.8:c.*492_*493dup	ENSP00000364080.4:n.*492_*493dup
ENST00000399079.7:c.*492_*493dup	ENSP00000382029.3:n.*492_*493dup
ENST00000399082.7:c.*492_*493dup	ENSP00000382032.3:n.*492_*493dup
ENST00000399084.5:c.*492_*493dup	ENSP00000382034.1:n.*492_*493dup
ENST00000434651.6:c.*492_*493dup	ENSP00000407332.2:n.*492_*493dup
ENST00000487676.1:n.4367_4368dup
NM_001243961.1:c.*492_*493dup	NP_001230890.1:n.*492_*493dup
NM_002123.4:c.*492_*493dup	NP_002114.3:n.*492_*493dup
NM_001243961.2:c.*492_*493dup	NP_001230890.1:n.*492_*493dup
NM_002123.5:c.*492_*493dup MANE Select	NP_002114.3:n.*492_*493dup