Canonical Allele Identifier: CA414781034
Gene: MT-CO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.5967T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5967T>C , J01415.2:m.5967T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.64T>C ENSP00000354499.2:p.Phe22Leu
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