Canonical Allele Identifier: CA2677950585
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270161-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270161A>C , CM000668.2:g.31270161A>C GRCh38
NC_000006.11:g.31237938A>C , CM000668.1:g.31237938A>C GRCh37
NC_000006.10:g.31345917A>C NCBI36
NG_029422.2:g.6971T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.895+49T>G MANE Select ENSP00000365402.5:n.895+49T>G
ENST00000376228.9:c.895+49T>G ENSP00000365402.5:n.895+49T>G
ENST00000376237.8:c.*482+49T>G ENSP00000365412.4:n.*482+49T>G
ENST00000383329.7:c.895+49T>G ENSP00000372819.3:n.895+49T>G
ENST00000470363.5:n.213+49T>G
ENST00000487245.5:n.1254+49T>G
NM_002117.5:c.895+49T>G NP_002108.4:n.895+49T>G
NM_002117.6:c.895+49T>G MANE Select NP_002108.4:n.895+49T>G
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