Canonical Allele Identifier: CA414775463

Gene: MT-ND2

Linked Data

• ClinVar Variation Id: 692486
• ClinVar RCV Id: RCV000853802
• dbSNP Id: rs1603219578
• MyVariant Identifiers: chrMT:g.4717A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4717A>T , J01415.2:m.4717A>T	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361453.3:c.248A>T	ENSP00000355046.4:p.Gln83Leu