Canonical Allele Identifier: CA414791422
Gene: MT-CO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.7129A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7129A>T , J01415.2:m.7129A>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361624.2:c.1226A>T ENSP00000354499.2:p.Tyr409Phe