Canonical Allele Identifier: CA414775553
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1328512
ClinVar RCV Id: RCV001796953
dbSNP Id: rs1603219589
MyVariant Identifiers: chrMT:g.4735C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4735C>G , J01415.2:m.4735C>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.266C>G ENSP00000355046.4:p.Thr89Ser