Canonical Allele Identifier: CA414779663
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.5284A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5284A>G , J01415.2:m.5284A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.815A>G ENSP00000355046.4:p.Lys272Arg