Canonical Allele Identifier: CA449790486
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31271663-G-C
gnomAD v4: 6-31271663-G-C
MyVariant Identifiers: chr6:g.31239440G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271663G>C , CM000668.2:g.31271663G>C GRCh38
NC_000006.11:g.31239440G>C , CM000668.1:g.31239440G>C GRCh37
NC_000006.10:g.31347419G>C NCBI36
NG_029422.2:g.5469C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.279C>G MANE Select ENSP00000365402.5:p.Arg93=
ENST00000376228.9:c.279C>G ENSP00000365402.5:p.Arg93=
ENST00000376237.8:c.279C>G ENSP00000365412.4:p.Arg93=
ENST00000383329.7:c.279C>G ENSP00000372819.3:p.Arg93=
ENST00000415537.1:c.277C>G
ENST00000484378.1:n.298C>G
ENST00000487245.5:n.388C>G
ENST00000495835.1:n.468C>G
NM_002117.5:c.279C>G NP_002108.4:p.Arg93=
NM_002117.6:c.279C>G MANE Select NP_002108.4:p.Arg93=
Search 100 bp 5'
Search 100 bp 3'