Canonical Allele Identifier: CA1619077317
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761102049
gnomAD v4: 6-31269087-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269087G>T , CM000668.2:g.31269087G>T GRCh38
NC_000006.11:g.31236864G>T , CM000668.1:g.31236864G>T GRCh37
NC_000006.10:g.31344843G>T NCBI36
NG_029422.2:g.8045C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*82C>A MANE Select ENSP00000365402.5:n.*82C>A
ENST00000376228.9:c.*82C>A ENSP00000365402.5:n.*82C>A
ENST00000376237.8:c.*770C>A ENSP00000365412.4:n.*770C>A
ENST00000383329.7:c.*82C>A ENSP00000372819.3:n.*82C>A
ENST00000466892.5:n.416C>A
ENST00000470363.5:n.941C>A
ENST00000487245.5:n.1542C>A
NM_002117.5:c.*82C>A NP_002108.4:n.*82C>A
NM_002117.6:c.*82C>A MANE Select NP_002108.4:n.*82C>A
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