Canonical Allele Identifier: CA414780805
Gene: MT-CO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.5919T>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5919T= , J01415.2:m.5919T= GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.16T= ENSP00000354499.2:p.Ter6=