Canonical Allele Identifier: CA414775509

Gene: MT-ND2

Linked Data

• ClinVar Variation Id: 692488
• ClinVar RCV Id: RCV000853804
• dbSNP Id: rs1603219581
• MyVariant Identifiers: chrMT:g.4725A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4725A>T , J01415.2:m.4725A>T	GRCh38

Transcript Alleles

HGVS	Amino-acid change
ENST00000361453.3:c.256A>T	ENSP00000355046.4:p.Ile86Leu