Canonical Allele Identifier: CA414775598
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.4746T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4746T>G , J01415.2:m.4746T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.277T>G ENSP00000355046.4:p.Tyr93Asp