Canonical Allele Identifier: CA414784307
Gene: MT-CO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.6487T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6487T>G , J01415.2:m.6487T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.584T>G ENSP00000354499.2:p.Leu195Arg