Canonical Allele Identifier: CA363319451
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269511-T-C
gnomAD v4: 6-31269511-T-C
MyVariant Identifiers: chr6:g.31237288T>C (hg19) chr6:g.31269511T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269511T>C , CM000668.2:g.31269511T>C GRCh38
NC_000006.11:g.31237288T>C , CM000668.1:g.31237288T>C GRCh37
NC_000006.10:g.31345267T>C NCBI36
NG_029422.2:g.7621A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1030A>G MANE Select ENSP00000365402.5:p.Ser344Gly
ENST00000376228.9:c.1030A>G ENSP00000365402.5:p.Ser344Gly
ENST00000376237.8:c.*617A>G ENSP00000365412.4:n.*617A>G
ENST00000383329.7:c.1048A>G ENSP00000372819.3:p.Ser350Gly
ENST00000466892.5:n.156A>G
ENST00000470363.5:n.788A>G
ENST00000487245.5:n.1389A>G
NM_002117.5:c.1030A>G NP_002108.4:p.Ser344Gly
NM_002117.6:c.1030A>G MANE Select NP_002108.4:p.Ser344Gly
Search 100 bp 5'
Search 100 bp 3'