Canonical Allele Identifier: CA414784259
Gene: MT-CO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.6478C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6478C>G , J01415.2:m.6478C>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.575C>G ENSP00000354499.2:p.Ala192Gly
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