Canonical Allele Identifier: CA2677949048
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31268874-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268874A>G , CM000668.2:g.31268874A>G GRCh38
NC_000006.11:g.31236651A>G , CM000668.1:g.31236651A>G GRCh37
NC_000006.10:g.31344630A>G NCBI36
NG_029422.2:g.8258T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*295T>C MANE Select ENSP00000365402.5:n.*295T>C
ENST00000376228.9:c.*295T>C ENSP00000365402.5:n.*295T>C
ENST00000376237.8:c.*983T>C ENSP00000365412.4:n.*983T>C
ENST00000383329.7:c.*295T>C ENSP00000372819.3:n.*295T>C
ENST00000466892.5:n.629T>C
ENST00000470363.5:n.1154T>C
ENST00000487245.5:n.1755T>C
NM_002117.5:c.*295T>C NP_002108.4:n.*295T>C
NM_002117.6:c.*295T>C MANE Select NP_002108.4:n.*295T>C
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