Canonical Allele Identifier: CA136953082

Gene: HLA-DQB1

Linked Data

• dbSNP Id: rs765291761
• gnomAD v2: 6-32627521-T-TTG
• gnomAD v3: 6-32659744-T-TTG
• gnomAD v4: 6-32659744-T-TTG
• MyVariant Identifiers: chr6:g.32627521_32627522insTG (hg19) ; chr6:g.32659744_32659745insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659744_32659745insTG , CM000668.2:g.32659744_32659745insTG	GRCh38
NC_000006.11:g.32627521_32627522insTG , CM000668.1:g.32627521_32627522insTG	GRCh37
NC_000006.10:g.32735499_32735500insTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*491_*492insCA MANE Select	ENSP00000407332.2:n.*491_*492insCA
ENST00000374943.8:c.*491_*492insCA	ENSP00000364080.4:n.*491_*492insCA
ENST00000399079.7:c.*491_*492insCA	ENSP00000382029.3:n.*491_*492insCA
ENST00000399082.7:c.*491_*492insCA	ENSP00000382032.3:n.*491_*492insCA
ENST00000399084.5:c.*491_*492insCA	ENSP00000382034.1:n.*491_*492insCA
ENST00000434651.6:c.*491_*492insCA	ENSP00000407332.2:n.*491_*492insCA
ENST00000487676.1:n.4366_4367insCA
NM_001243961.1:c.*491_*492insCA	NP_001230890.1:n.*491_*492insCA
NM_002123.4:c.*491_*492insCA	NP_002114.3:n.*491_*492insCA
NM_001243961.2:c.*491_*492insCA	NP_001230890.1:n.*491_*492insCA
NM_002123.5:c.*491_*492insCA MANE Select	NP_002114.3:n.*491_*492insCA