Canonical Allele Identifier: CA337096913
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs372070966
MyVariant Identifiers: chrMT:g.4586T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4586T>C , J01415.2:m.4586T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.117T>C ENSP00000355046.4:p.Ala39=