Canonical Allele Identifier: CA1619077102
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761077921
gnomAD v4: 6-31268799-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268799A>C , CM000668.2:g.31268799A>C GRCh38
NC_000006.11:g.31236576A>C , CM000668.1:g.31236576A>C GRCh37
NC_000006.10:g.31344555A>C NCBI36
NG_029422.2:g.8333T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*370T>G MANE Select ENSP00000365402.5:n.*370T>G
ENST00000376228.9:c.*370T>G ENSP00000365402.5:n.*370T>G
ENST00000376237.8:c.*1058T>G ENSP00000365412.4:n.*1058T>G
ENST00000383329.7:c.*370T>G ENSP00000372819.3:n.*370T>G
ENST00000466892.5:n.704T>G
ENST00000470363.5:n.1229T>G
ENST00000487245.5:n.1830T>G
NM_002117.5:c.*370T>G NP_002108.4:n.*370T>G
NM_002117.6:c.*370T>G MANE Select NP_002108.4:n.*370T>G
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