Canonical Allele Identifier: CA449790265
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271116-G-C
MyVariant Identifiers: chr6:g.31238893G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271116G>C , CM000668.2:g.31271116G>C GRCh38
NC_000006.11:g.31238893G>C , CM000668.1:g.31238893G>C GRCh37
NC_000006.10:g.31346872G>C NCBI36
NG_029422.2:g.6016C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.576C>G MANE Select ENSP00000365402.5:p.Leu192=
ENST00000376228.9:c.576C>G ENSP00000365402.5:p.Leu192=
ENST00000376237.8:c.*163C>G ENSP00000365412.4:n.*163C>G
ENST00000383329.7:c.576C>G ENSP00000372819.3:p.Leu192=
ENST00000415537.1:c.574C>G
ENST00000484378.1:n.845C>G
ENST00000487245.5:n.935C>G
ENST00000495835.1:n.765C>G
NM_002117.5:c.576C>G NP_002108.4:p.Leu192=
NM_002117.6:c.576C>G MANE Select NP_002108.4:p.Leu192=
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Search 100 bp 3'