Canonical Allele Identifier: CA414779638
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.5279C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5279C>A , J01415.2:m.5279C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.810C>A ENSP00000355046.4:p.Phe270Leu