Canonical Allele Identifier: CA12441670
Gene: HLA-DQB1 HGNC NCBI
HLA-DQB1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1049222
gnomAD v2: 6-32627752-T-C
gnomAD v3: 6-32659975-T-C
gnomAD v4: 6-32659975-T-C
MyVariant Identifiers: chr6:g.32627752T>C (hg19) chr6:g.32659975T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32659975T>C , CM000668.2:g.32659975T>C GRCh38
NC_000006.11:g.32627752T>C , CM000668.1:g.32627752T>C GRCh37
NC_000006.10:g.32735730T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000434651.7:c.*261A>G (HLA-DQB1) MANE Select ENSP00000407332.2:n.*261A>G
ENST00000374943.8:c.*261A>G (HLA-DQB1) ENSP00000364080.4:n.*261A>G
ENST00000399079.7:c.*261A>G (HLA-DQB1) ENSP00000382029.3:n.*261A>G
ENST00000399082.7:c.*261A>G (HLA-DQB1) ENSP00000382032.3:n.*261A>G
ENST00000399084.5:c.*261A>G (HLA-DQB1) ENSP00000382034.1:n.*261A>G
ENST00000434651.6:c.*261A>G (HLA-DQB1) ENSP00000407332.2:n.*261A>G
ENST00000443574.1:n.220A>G (HLA-DQB1)
ENST00000460185.1:n.339A>G (HLA-DQB1)
ENST00000487676.1:n.4136A>G (HLA-DQB1)
NM_001243961.1:c.*261A>G (HLA-DQB1) NP_001230890.1:n.*261A>G
NM_002123.4:c.*261A>G (HLA-DQB1) NP_002114.3:n.*261A>G
NR_133907.1:n.96T>C (HLA-DQB1-AS1)
NM_001243961.2:c.*261A>G (HLA-DQB1) NP_001230890.1:n.*261A>G
NM_002123.5:c.*261A>G (HLA-DQB1) MANE Select NP_002114.3:n.*261A>G
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