Canonical Allele Identifier: CA136860928
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs115510686
gnomAD v2: 6-31236590-T-C
gnomAD v3: 6-31268813-T-C
gnomAD v4: 6-31268813-T-C
MyVariant Identifiers: chr6:g.31236590T>C (hg19) chr6:g.31268813T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268813T>C , CM000668.2:g.31268813T>C GRCh38
NC_000006.11:g.31236590T>C , CM000668.1:g.31236590T>C GRCh37
NC_000006.10:g.31344569T>C NCBI36
NG_029422.2:g.8319A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*356A>G MANE Select ENSP00000365402.5:n.*356A>G
ENST00000376228.9:c.*356A>G ENSP00000365402.5:n.*356A>G
ENST00000376237.8:c.*1044A>G ENSP00000365412.4:n.*1044A>G
ENST00000383329.7:c.*356A>G ENSP00000372819.3:n.*356A>G
ENST00000466892.5:n.690A>G
ENST00000470363.5:n.1215A>G
ENST00000487245.5:n.1816A>G
NM_002117.5:c.*356A>G NP_002108.4:n.*356A>G
NM_002117.6:c.*356A>G MANE Select NP_002108.4:n.*356A>G
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