Canonical Allele Identifier: CA337097156
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs3020602
MyVariant Identifiers: chrMT:g.5495T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5495T>C , J01415.2:m.5495T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.1026T>C ENSP00000355046.4:p.Phe342=