Canonical Allele Identifier: CA1087616030
Gene: HLA-DQB1 HGNC NCBI

Linked Data

gnomAD v3: 6-32659714-T-TC
gnomAD v4: 6-32659714-T-TC
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32659714_32659715insC , CM000668.2:g.32659714_32659715insC GRCh38
NC_000006.11:g.32627491_32627492insC , CM000668.1:g.32627491_32627492insC GRCh37
NC_000006.10:g.32735469_32735470insC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000434651.7:c.*521_*522insG MANE Select ENSP00000407332.2:n.*521_*522insG
ENST00000374943.8:c.*521_*522insG ENSP00000364080.4:n.*521_*522insG
ENST00000399079.7:c.*521_*522insG ENSP00000382029.3:n.*521_*522insG
ENST00000399082.7:c.*521_*522insG ENSP00000382032.3:n.*521_*522insG
ENST00000399084.5:c.*521_*522insG ENSP00000382034.1:n.*521_*522insG
ENST00000434651.6:c.*521_*522insG ENSP00000407332.2:n.*521_*522insG
ENST00000487676.1:n.4396_4397insG
NM_001243961.1:c.*521_*522insG NP_001230890.1:n.*521_*522insG
NM_002123.4:c.*521_*522insG NP_002114.3:n.*521_*522insG
NM_001243961.2:c.*521_*522insG NP_001230890.1:n.*521_*522insG
NM_002123.5:c.*521_*522insG MANE Select NP_002114.3:n.*521_*522insG
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