Canonical Allele Identifier: CA414774591

Gene: MT-ND2

Linked Data

• ClinVar Variation Id: 692449
• ClinVar RCV Id: RCV000853764
• dbSNP Id: rs1603219477
• MyVariant Identifiers: chrMT:g.4494A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4494A>G , J01415.2:m.4494A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361453.3:c.25A>G	ENSP00000355046.4:p.Ile9Val