Canonical Allele Identifier: CA414774609
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692453
ClinVar RCV Id: RCV000853768
dbSNP Id: rs1603219484
MyVariant Identifiers: chrMT:g.4501C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4501C>T , J01415.2:m.4501C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.32C>T ENSP00000355046.4:p.Ser11Phe