Canonical Allele Identifier: CA2677949142
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31268930-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268930G>T , CM000668.2:g.31268930G>T GRCh38
NC_000006.11:g.31236707G>T , CM000668.1:g.31236707G>T GRCh37
NC_000006.10:g.31344686G>T NCBI36
NG_029422.2:g.8202C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*239C>A MANE Select ENSP00000365402.5:n.*239C>A
ENST00000376228.9:c.*239C>A ENSP00000365402.5:n.*239C>A
ENST00000376237.8:c.*927C>A ENSP00000365412.4:n.*927C>A
ENST00000383329.7:c.*239C>A ENSP00000372819.3:n.*239C>A
ENST00000466892.5:n.573C>A
ENST00000470363.5:n.1098C>A
ENST00000487245.5:n.1699C>A
NM_002117.5:c.*239C>A NP_002108.4:n.*239C>A
NM_002117.6:c.*239C>A MANE Select NP_002108.4:n.*239C>A
Search 100 bp 5'
Search 100 bp 3'