Canonical Allele Identifier: CA414775600

Gene: MT-ND2

Linked Data

• ClinVar Variation Id: 692495
• ClinVar RCV Id: RCV000853811
• dbSNP Id: rs1603219594
• MyVariant Identifiers: chrMT:g.4746T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4746T>C , J01415.2:m.4746T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361453.3:c.277T>C	ENSP00000355046.4:p.Tyr93His