Canonical Allele Identifier: CA2677950575
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270152-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270152T>G , CM000668.2:g.31270152T>G GRCh38
NC_000006.11:g.31237929T>G , CM000668.1:g.31237929T>G GRCh37
NC_000006.10:g.31345908T>G NCBI36
NG_029422.2:g.6980A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.895+58A>C MANE Select ENSP00000365402.5:n.895+58A>C
ENST00000376228.9:c.895+58A>C ENSP00000365402.5:n.895+58A>C
ENST00000376237.8:c.*482+58A>C ENSP00000365412.4:n.*482+58A>C
ENST00000383329.7:c.895+58A>C ENSP00000372819.3:n.895+58A>C
ENST00000470363.5:n.213+58A>C
ENST00000487245.5:n.1254+58A>C
NM_002117.5:c.895+58A>C NP_002108.4:n.895+58A>C
NM_002117.6:c.895+58A>C MANE Select NP_002108.4:n.895+58A>C
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