Canonical Allele Identifier: CA823861414
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs9281299
gnomAD v4: 6-31269750-A-AC
MyVariant Identifiers: chr6:g.31237527_31237528insC (hg19) chr6:g.31269750_31269751insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269750_31269751insC , CM000668.2:g.31269750_31269751insC GRCh38
NC_000006.11:g.31237527_31237528insC , CM000668.1:g.31237527_31237528insC GRCh37
NC_000006.10:g.31345506_31345507insC NCBI36
NG_029422.2:g.7381_7382insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+215_1015+216insG MANE Select ENSP00000365402.5:n.1015+215_1015+216insG
ENST00000376228.9:c.1015+215_1015+216insG ENSP00000365402.5:n.1015+215_1015+216insG
ENST00000376237.8:c.*602+215_*602+216insG ENSP00000365412.4:n.*602+215_*602+216insG
ENST00000383329.7:c.1016-208_1016-207insG ENSP00000372819.3:n.1016-208_1016-207insG
ENST00000470363.5:n.548_549insG
ENST00000487245.5:n.1374+215_1374+216insG
NM_002117.5:c.1015+215_1015+216insG NP_002108.4:n.1015+215_1015+216insG
NM_002117.6:c.1015+215_1015+216insG MANE Select NP_002108.4:n.1015+215_1015+216insG
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