Canonical Allele Identifier: CA414780018
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.5365C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5365C>T , J01415.2:m.5365C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.896C>T ENSP00000355046.4:p.Ser299Phe