Canonical Allele Identifier: CA414774753
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.4564G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4564G>A , J01415.2:m.4564G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.95G>A ENSP00000355046.4:p.Gly32Asp