Canonical Allele Identifier: CA414780619

Gene: MT-ND2

Linked Data

• ClinVar Variation Id: 585066
• ClinVar RCV Id: RCV000709825 ; RCV000853916
• dbSNP Id: rs1569484003
• MyVariant Identifiers: chrMT:g.5505A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5505A>G , J01415.2:m.5505A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361453.3:c.1036A>G	ENSP00000355046.4:p.Ile346Val