Canonical Allele Identifier: CA414791444
Gene: MT-CO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.7132C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7132C>G , J01415.2:m.7132C>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361624.2:c.1229C>G ENSP00000354499.2:p.Ala410Gly