Canonical Allele Identifier: CA363319515
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269539-A-T
gnomAD v4: 6-31269539-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269539A>T , CM000668.2:g.31269539A>T GRCh38
NC_000006.11:g.31237316A>T , CM000668.1:g.31237316A>T GRCh37
NC_000006.10:g.31345295A>T NCBI36
NG_029422.2:g.7593T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-14T>A MANE Select ENSP00000365402.5:n.1016-14T>A
ENST00000376228.9:c.1016-14T>A ENSP00000365402.5:n.1016-14T>A
ENST00000376237.8:c.*603-14T>A ENSP00000365412.4:n.*603-14T>A
ENST00000383329.7:c.1020T>A ENSP00000372819.3:p.His340Gln
ENST00000466892.5:n.128T>A
ENST00000470363.5:n.760T>A
ENST00000487245.5:n.1375-14T>A
NM_002117.5:c.1016-14T>A NP_002108.4:n.1016-14T>A
NM_002117.6:c.1016-14T>A MANE Select NP_002108.4:n.1016-14T>A