Canonical Allele Identifier: CA414781200
Gene: MT-CO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.6006C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6006C>T , J01415.2:m.6006C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361624.2:c.103C>T ENSP00000354499.2:p.Leu35Phe
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