Canonical Allele Identifier: CA414774609

Gene: MT-ND2

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