Canonical Allele Identifier: CA136952881

Gene: HLA-DQB1

Linked Data

• dbSNP Id: rs9273415
• gnomAD v2: 6-32627310-C-T
• gnomAD v3: 6-32659533-C-T
• gnomAD v4: 6-32659533-C-T
• MyVariant Identifiers: chr6:g.32627310C>T (hg19) ; chr6:g.32659533C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659533C>T , CM000668.2:g.32659533C>T	GRCh38
NC_000006.11:g.32627310C>T , CM000668.1:g.32627310C>T	GRCh37
NC_000006.10:g.32735288C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*703G>A MANE Select	ENSP00000407332.2:n.*703G>A
ENST00000374943.8:c.*703G>A	ENSP00000364080.4:n.*703G>A
ENST00000399079.7:c.*703G>A	ENSP00000382029.3:n.*703G>A
ENST00000399082.7:c.*703G>A	ENSP00000382032.3:n.*703G>A
ENST00000399084.5:c.*703G>A	ENSP00000382034.1:n.*703G>A
ENST00000434651.6:c.*703G>A	ENSP00000407332.2:n.*703G>A
ENST00000487676.1:n.4578G>A
NM_001243961.1:c.*703G>A	NP_001230890.1:n.*703G>A
NM_002123.4:c.*703G>A	NP_002114.3:n.*703G>A
NM_001243961.2:c.*703G>A	NP_001230890.1:n.*703G>A
NM_002123.5:c.*703G>A MANE Select	NP_002114.3:n.*703G>A