Canonical Allele Identifier: CA2677949342
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269072-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269072T>A , CM000668.2:g.31269072T>A GRCh38
NC_000006.11:g.31236849T>A , CM000668.1:g.31236849T>A GRCh37
NC_000006.10:g.31344828T>A NCBI36
NG_029422.2:g.8060A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*97A>T MANE Select ENSP00000365402.5:n.*97A>T
ENST00000376228.9:c.*97A>T ENSP00000365402.5:n.*97A>T
ENST00000376237.8:c.*785A>T ENSP00000365412.4:n.*785A>T
ENST00000383329.7:c.*97A>T ENSP00000372819.3:n.*97A>T
ENST00000466892.5:n.431A>T
ENST00000470363.5:n.956A>T
ENST00000487245.5:n.1557A>T
NM_002117.5:c.*97A>T NP_002108.4:n.*97A>T
NM_002117.6:c.*97A>T MANE Select NP_002108.4:n.*97A>T