Canonical Allele Identifier: CA449744165
Gene: HLA-DQB1 HGNC NCBI
HLA-DQB1-AS1 HGNC NCBI

Linked Data

gnomAD v4: 6-32659934-A-G
MyVariant Identifiers: chr6:g.32627711A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32659934A>G , CM000668.2:g.32659934A>G GRCh38
NC_000006.11:g.32627711A>G , CM000668.1:g.32627711A>G GRCh37
NC_000006.10:g.32735689A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000434651.7:c.*302T>C (HLA-DQB1) MANE Select ENSP00000407332.2:n.*302T>C
ENST00000374943.8:c.*302T>C (HLA-DQB1) ENSP00000364080.4:n.*302T>C
ENST00000399079.7:c.*302T>C (HLA-DQB1) ENSP00000382029.3:n.*302T>C
ENST00000399082.7:c.*302T>C (HLA-DQB1) ENSP00000382032.3:n.*302T>C
ENST00000399084.5:c.*302T>C (HLA-DQB1) ENSP00000382034.1:n.*302T>C
ENST00000434651.6:c.*302T>C (HLA-DQB1) ENSP00000407332.2:n.*302T>C
ENST00000443574.1:n.261T>C (HLA-DQB1)
ENST00000460185.1:n.380T>C (HLA-DQB1)
ENST00000487676.1:n.4177T>C (HLA-DQB1)
NM_001243961.1:c.*302T>C (HLA-DQB1) NP_001230890.1:n.*302T>C
NM_002123.4:c.*302T>C (HLA-DQB1) NP_002114.3:n.*302T>C
NR_133907.1:n.55A>G (HLA-DQB1-AS1)
NM_001243961.2:c.*302T>C (HLA-DQB1) NP_001230890.1:n.*302T>C
NM_002123.5:c.*302T>C (HLA-DQB1) MANE Select NP_002114.3:n.*302T>C
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