Canonical Allele Identifier: CA414775458
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.4716C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4716C>T , J01415.2:m.4716C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.247C>T ENSP00000355046.4:p.Gln83Ter