Canonical Allele Identifier: CA15475781

Gene: HLA-DQB1

Linked Data

• dbSNP Id: rs9273440
• gnomAD v2: 6-32627561-T-C
• gnomAD v3: 6-32659784-T-C
• gnomAD v4: 6-32659784-T-C
• MyVariant Identifiers: chr6:g.32627561T>C (hg19) ; chr6:g.32659784T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659784T>C , CM000668.2:g.32659784T>C	GRCh38
NC_000006.11:g.32627561T>C , CM000668.1:g.32627561T>C	GRCh37
NC_000006.10:g.32735539T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*452A>G MANE Select	ENSP00000407332.2:n.*452A>G
ENST00000374943.8:c.*452A>G	ENSP00000364080.4:n.*452A>G
ENST00000399079.7:c.*452A>G	ENSP00000382029.3:n.*452A>G
ENST00000399082.7:c.*452A>G	ENSP00000382032.3:n.*452A>G
ENST00000399084.5:c.*452A>G	ENSP00000382034.1:n.*452A>G
ENST00000434651.6:c.*452A>G	ENSP00000407332.2:n.*452A>G
ENST00000487676.1:n.4327A>G
NM_001243961.1:c.*452A>G	NP_001230890.1:n.*452A>G
NM_002123.4:c.*452A>G	NP_002114.3:n.*452A>G
NM_001243961.2:c.*452A>G	NP_001230890.1:n.*452A>G
NM_002123.5:c.*452A>G MANE Select	NP_002114.3:n.*452A>G