Canonical Allele Identifier: CA414780399
Gene: MT-ND2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.5449C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5449C>T , J01415.2:m.5449C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.980C>T ENSP00000355046.4:p.Pro327Leu