Canonical Allele Identifier: CA1087450378
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269442-A-T
gnomAD v4: 6-31269442-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269442A>T , CM000668.2:g.31269442A>T GRCh38
NC_000006.11:g.31237219A>T , CM000668.1:g.31237219A>T GRCh37
NC_000006.10:g.31345198A>T NCBI36
NG_029422.2:g.7690T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1048+51T>A MANE Select ENSP00000365402.5:n.1048+51T>A
ENST00000376228.9:c.1048+51T>A ENSP00000365402.5:n.1048+51T>A
ENST00000376237.8:c.*635+51T>A ENSP00000365412.4:n.*635+51T>A
ENST00000383329.7:c.1066+51T>A ENSP00000372819.3:n.1066+51T>A
ENST00000466892.5:n.225T>A
ENST00000470363.5:n.806+51T>A
ENST00000487245.5:n.1407+51T>A
NM_002117.5:c.1048+51T>A NP_002108.4:n.1048+51T>A
NM_002117.6:c.1048+51T>A MANE Select NP_002108.4:n.1048+51T>A