Canonical Allele Identifier: CA363320462
Gene: HLA-C HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31238031T>C (hg19) chr6:g.31270254T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270254T>C , CM000668.2:g.31270254T>C GRCh38
NC_000006.11:g.31238031T>C , CM000668.1:g.31238031T>C GRCh37
NC_000006.10:g.31346010T>C NCBI36
NG_029422.2:g.6878A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.851A>G MANE Select ENSP00000365402.5:p.His284Arg
ENST00000376228.9:c.851A>G ENSP00000365402.5:p.His284Arg
ENST00000376237.8:c.*438A>G ENSP00000365412.4:n.*438A>G
ENST00000383329.7:c.851A>G ENSP00000372819.3:p.His284Arg
ENST00000415537.1:c.742A>G
ENST00000470363.5:n.169A>G
ENST00000487245.5:n.1210A>G
ENST00000495835.1:n.1040A>G
NM_002117.5:c.851A>G NP_002108.4:p.His284Arg
NM_002117.6:c.851A>G MANE Select NP_002108.4:p.His284Arg
Search 100 bp 5'
Search 100 bp 3'