Canonical Allele Identifier: CA2677951511
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271467-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271467G>T , CM000668.2:g.31271467G>T GRCh38
NC_000006.11:g.31239244G>T , CM000668.1:g.31239244G>T GRCh37
NC_000006.10:g.31347223G>T NCBI36
NG_029422.2:g.5665C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-119C>A MANE Select ENSP00000365402.5:n.344-119C>A
ENST00000376228.9:c.344-119C>A ENSP00000365402.5:n.344-119C>A
ENST00000376237.8:c.343+132C>A ENSP00000365412.4:n.343+132C>A
ENST00000383329.7:c.344-119C>A ENSP00000372819.3:n.344-119C>A
ENST00000415537.1:c.342-119C>A
ENST00000484378.1:n.494C>A
ENST00000487245.5:n.584C>A
ENST00000495835.1:n.533-119C>A
NM_002117.5:c.344-119C>A NP_002108.4:n.344-119C>A
NM_002117.6:c.344-119C>A MANE Select NP_002108.4:n.344-119C>A
Search 100 bp 5'
Search 100 bp 3'