Canonical Allele Identifier: CA2677950978
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270729-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270729G>C , CM000668.2:g.31270729G>C GRCh38
NC_000006.11:g.31238506G>C , CM000668.1:g.31238506G>C GRCh37
NC_000006.10:g.31346485G>C NCBI36
NG_029422.2:g.6403C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-244C>G MANE Select ENSP00000365402.5:n.620-244C>G
ENST00000376228.9:c.620-244C>G ENSP00000365402.5:n.620-244C>G
ENST00000376237.8:c.*207-244C>G ENSP00000365412.4:n.*207-244C>G
ENST00000383329.7:c.620-244C>G ENSP00000372819.3:n.620-244C>G
ENST00000415537.1:c.618-244C>G
ENST00000487245.5:n.979-244C>G
ENST00000495835.1:n.809-244C>G
NM_002117.5:c.620-244C>G NP_002108.4:n.620-244C>G
NM_002117.6:c.620-244C>G MANE Select NP_002108.4:n.620-244C>G
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