Canonical Allele Identifier: CA2677949419
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269111-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269111A>T , CM000668.2:g.31269111A>T GRCh38
NC_000006.11:g.31236888A>T , CM000668.1:g.31236888A>T GRCh37
NC_000006.10:g.31344867A>T NCBI36
NG_029422.2:g.8021T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*58T>A MANE Select ENSP00000365402.5:n.*58T>A
ENST00000376228.9:c.*58T>A ENSP00000365402.5:n.*58T>A
ENST00000376237.8:c.*746T>A ENSP00000365412.4:n.*746T>A
ENST00000383329.7:c.*58T>A ENSP00000372819.3:n.*58T>A
ENST00000466892.5:n.392T>A
ENST00000470363.5:n.917T>A
ENST00000487245.5:n.1518T>A
NM_002117.5:c.*58T>A NP_002108.4:n.*58T>A
NM_002117.6:c.*58T>A MANE Select NP_002108.4:n.*58T>A