Canonical Allele Identifier: CA1087452118
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269881-A-T
gnomAD v4: 6-31269881-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269881A>T , CM000668.2:g.31269881A>T GRCh38
NC_000006.11:g.31237658A>T , CM000668.1:g.31237658A>T GRCh37
NC_000006.10:g.31345637A>T NCBI36
NG_029422.2:g.7251T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+85T>A MANE Select ENSP00000365402.5:n.1015+85T>A
ENST00000376228.9:c.1015+85T>A ENSP00000365402.5:n.1015+85T>A
ENST00000376237.8:c.*602+85T>A ENSP00000365412.4:n.*602+85T>A
ENST00000383329.7:c.1015+85T>A ENSP00000372819.3:n.1015+85T>A
ENST00000470363.5:n.418T>A
ENST00000487245.5:n.1374+85T>A
NM_002117.5:c.1015+85T>A NP_002108.4:n.1015+85T>A
NM_002117.6:c.1015+85T>A MANE Select NP_002108.4:n.1015+85T>A