Canonical Allele Identifier: CA136953024

Gene: HLA-DQB1

Linked Data

• dbSNP Id: rs9273432
• gnomAD v2: 6-32627485-T-C
• gnomAD v3: 6-32659708-T-C
• gnomAD v4: 6-32659708-T-C
• MyVariant Identifiers: chr6:g.32627485T>C (hg19) ; chr6:g.32659708T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659708T>C , CM000668.2:g.32659708T>C	GRCh38
NC_000006.11:g.32627485T>C , CM000668.1:g.32627485T>C	GRCh37
NC_000006.10:g.32735463T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*528A>G MANE Select	ENSP00000407332.2:n.*528A>G
ENST00000374943.8:c.*528A>G	ENSP00000364080.4:n.*528A>G
ENST00000399079.7:c.*528A>G	ENSP00000382029.3:n.*528A>G
ENST00000399082.7:c.*528A>G	ENSP00000382032.3:n.*528A>G
ENST00000399084.5:c.*528A>G	ENSP00000382034.1:n.*528A>G
ENST00000434651.6:c.*528A>G	ENSP00000407332.2:n.*528A>G
ENST00000487676.1:n.4403A>G
NM_001243961.1:c.*528A>G	NP_001230890.1:n.*528A>G
NM_002123.4:c.*528A>G	NP_002114.3:n.*528A>G
NM_001243961.2:c.*528A>G	NP_001230890.1:n.*528A>G
NM_002123.5:c.*528A>G MANE Select	NP_002114.3:n.*528A>G