Canonical Allele Identifier: CA1087615823

Gene: HLA-DQB1

Linked Data

• gnomAD v3: 6-32659486-T-TCC
• gnomAD v4: 6-32659486-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659486_32659487insCC , CM000668.2:g.32659486_32659487insCC	GRCh38
NC_000006.11:g.32627263_32627264insCC , CM000668.1:g.32627263_32627264insCC	GRCh37
NC_000006.10:g.32735241_32735242insCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*749_*750insGG MANE Select	ENSP00000407332.2:n.*749_*750insGG
ENST00000374943.8:c.*749_*750insGG	ENSP00000364080.4:n.*749_*750insGG
ENST00000399079.7:c.*749_*750insGG	ENSP00000382029.3:n.*749_*750insGG
ENST00000399082.7:c.*749_*750insGG	ENSP00000382032.3:n.*749_*750insGG
ENST00000399084.5:c.*749_*750insGG	ENSP00000382034.1:n.*749_*750insGG
ENST00000434651.6:c.*749_*750insGG	ENSP00000407332.2:n.*749_*750insGG
ENST00000487676.1:n.4624_4625insGG
NM_001243961.1:c.*749_*750insGG	NP_001230890.1:n.*749_*750insGG
NM_002123.4:c.*749_*750insGG	NP_002114.3:n.*749_*750insGG
NM_001243961.2:c.*749_*750insGG	NP_001230890.1:n.*749_*750insGG
NM_002123.5:c.*749_*750insGG MANE Select	NP_002114.3:n.*749_*750insGG