Canonical Allele Identifier: CA414775520

Gene: MT-ND2

Linked Data

• ClinVar Variation Id: 692490
• ClinVar RCV Id: RCV000853806
• dbSNP Id: rs1556422892
• MyVariant Identifiers: chrMT:g.4728A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4728A>G , J01415.2:m.4728A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361453.3:c.259A>G	ENSP00000355046.4:p.Thr87Ala