Canonical Allele Identifier: CA1087448695
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31268820-A-T
gnomAD v4: 6-31268820-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268820A>T , CM000668.2:g.31268820A>T GRCh38
NC_000006.11:g.31236597A>T , CM000668.1:g.31236597A>T GRCh37
NC_000006.10:g.31344576A>T NCBI36
NG_029422.2:g.8312T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*349T>A MANE Select ENSP00000365402.5:n.*349T>A
ENST00000376228.9:c.*349T>A ENSP00000365402.5:n.*349T>A
ENST00000376237.8:c.*1037T>A ENSP00000365412.4:n.*1037T>A
ENST00000383329.7:c.*349T>A ENSP00000372819.3:n.*349T>A
ENST00000466892.5:n.683T>A
ENST00000470363.5:n.1208T>A
ENST00000487245.5:n.1809T>A
NM_002117.5:c.*349T>A NP_002108.4:n.*349T>A
NM_002117.6:c.*349T>A MANE Select NP_002108.4:n.*349T>A
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