Canonical Allele Identifier: CA414780376
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.5444C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5444C>G , J01415.2:m.5444C>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.975C>G ENSP00000355046.4:p.Phe325Leu