Canonical Allele Identifier: CA1087448692
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31268803-A-T
gnomAD v4: 6-31268803-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268803A>T , CM000668.2:g.31268803A>T GRCh38
NC_000006.11:g.31236580A>T , CM000668.1:g.31236580A>T GRCh37
NC_000006.10:g.31344559A>T NCBI36
NG_029422.2:g.8329T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*366T>A MANE Select ENSP00000365402.5:n.*366T>A
ENST00000376228.9:c.*366T>A ENSP00000365402.5:n.*366T>A
ENST00000376237.8:c.*1054T>A ENSP00000365412.4:n.*1054T>A
ENST00000383329.7:c.*366T>A ENSP00000372819.3:n.*366T>A
ENST00000466892.5:n.700T>A
ENST00000470363.5:n.1225T>A
ENST00000487245.5:n.1826T>A
NM_002117.5:c.*366T>A NP_002108.4:n.*366T>A
NM_002117.6:c.*366T>A MANE Select NP_002108.4:n.*366T>A