Canonical Allele Identifier: CA414779633
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.5278T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5278T>A , J01415.2:m.5278T>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.809T>A ENSP00000355046.4:p.Phe270Tyr