Canonical Allele Identifier: CA1087451106
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269563-A-C
gnomAD v4: 6-31269563-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269563A>C , CM000668.2:g.31269563A>C GRCh38
NC_000006.11:g.31237340A>C , CM000668.1:g.31237340A>C GRCh37
NC_000006.10:g.31345319A>C NCBI36
NG_029422.2:g.7569T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-38T>G MANE Select ENSP00000365402.5:n.1016-38T>G
ENST00000376228.9:c.1016-38T>G ENSP00000365402.5:n.1016-38T>G
ENST00000376237.8:c.*603-38T>G ENSP00000365412.4:n.*603-38T>G
ENST00000383329.7:c.1016-20T>G ENSP00000372819.3:n.1016-20T>G
ENST00000466892.5:n.104T>G
ENST00000470363.5:n.736T>G
ENST00000487245.5:n.1375-38T>G
NM_002117.5:c.1016-38T>G NP_002108.4:n.1016-38T>G
NM_002117.6:c.1016-38T>G MANE Select NP_002108.4:n.1016-38T>G