Canonical Allele Identifier: CA2677949207
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31268976-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268976G>T , CM000668.2:g.31268976G>T GRCh38
NC_000006.11:g.31236753G>T , CM000668.1:g.31236753G>T GRCh37
NC_000006.10:g.31344732G>T NCBI36
NG_029422.2:g.8156C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*193C>A MANE Select ENSP00000365402.5:n.*193C>A
ENST00000376228.9:c.*193C>A ENSP00000365402.5:n.*193C>A
ENST00000376237.8:c.*881C>A ENSP00000365412.4:n.*881C>A
ENST00000383329.7:c.*193C>A ENSP00000372819.3:n.*193C>A
ENST00000466892.5:n.527C>A
ENST00000470363.5:n.1052C>A
ENST00000487245.5:n.1653C>A
NM_002117.5:c.*193C>A NP_002108.4:n.*193C>A
NM_002117.6:c.*193C>A MANE Select NP_002108.4:n.*193C>A