Canonical Allele Identifier: CA1087449580
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269273-T-C
gnomAD v4: 6-31269273-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269273T>C , CM000668.2:g.31269273T>C GRCh38
NC_000006.11:g.31237050T>C , CM000668.1:g.31237050T>C GRCh37
NC_000006.10:g.31345029T>C NCBI36
NG_029422.2:g.7859A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1096+65A>G MANE Select ENSP00000365402.5:n.1096+65A>G
ENST00000376228.9:c.1096+65A>G ENSP00000365402.5:n.1096+65A>G
ENST00000376237.8:c.*683+65A>G ENSP00000365412.4:n.*683+65A>G
ENST00000383329.7:c.1114+65A>G ENSP00000372819.3:n.1114+65A>G
ENST00000466892.5:n.329+65A>G
ENST00000470363.5:n.854+65A>G
ENST00000487245.5:n.1455+65A>G
NM_002117.5:c.1096+65A>G NP_002108.4:n.1096+65A>G
NM_002117.6:c.1096+65A>G MANE Select NP_002108.4:n.1096+65A>G