Canonical Allele Identifier: CA449744279

Gene: HLA-DQB1 HLA-DQB1-AS1

Linked Data

• gnomAD v4: 6-32659974-A-C
• MyVariant Identifiers: chr6:g.32627751A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659974A>C , CM000668.2:g.32659974A>C	GRCh38
NC_000006.11:g.32627751A>C , CM000668.1:g.32627751A>C	GRCh37
NC_000006.10:g.32735729A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000434651.7:c.*262T>G (HLA-DQB1) MANE Select	ENSP00000407332.2:n.*262T>G
ENST00000374943.8:c.*262T>G (HLA-DQB1)	ENSP00000364080.4:n.*262T>G
ENST00000399079.7:c.*262T>G (HLA-DQB1)	ENSP00000382029.3:n.*262T>G
ENST00000399082.7:c.*262T>G (HLA-DQB1)	ENSP00000382032.3:n.*262T>G
ENST00000399084.5:c.*262T>G (HLA-DQB1)	ENSP00000382034.1:n.*262T>G
ENST00000434651.6:c.*262T>G (HLA-DQB1)	ENSP00000407332.2:n.*262T>G
ENST00000443574.1:n.221T>G (HLA-DQB1)
ENST00000460185.1:n.340T>G (HLA-DQB1)
ENST00000487676.1:n.4137T>G (HLA-DQB1)
NM_001243961.1:c.*262T>G (HLA-DQB1)	NP_001230890.1:n.*262T>G
NM_002123.4:c.*262T>G (HLA-DQB1)	NP_002114.3:n.*262T>G
NR_133907.1:n.95A>C (HLA-DQB1-AS1)
NM_001243961.2:c.*262T>G (HLA-DQB1)	NP_001230890.1:n.*262T>G
NM_002123.5:c.*262T>G (HLA-DQB1) MANE Select	NP_002114.3:n.*262T>G