Canonical Allele Identifier: CA414781202
Gene: MT-CO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.6007T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6007T>A , J01415.2:m.6007T>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361624.2:c.104T>A ENSP00000354499.2:p.Leu35His
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