Canonical Allele Identifier: CA414783522
Gene: MT-CO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.6369T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6369T>G , J01415.2:m.6369T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.466T>G ENSP00000354499.2:p.Ser156Ala
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