Canonical Allele Identifier: CA414775551

Gene: MT-ND2

Linked Data

• ClinVar Variation Id: 692493
• ClinVar RCV Id: RCV000853809
• dbSNP Id: rs1603219589
• MyVariant Identifiers: chrMT:g.4735C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4735C>A , J01415.2:m.4735C>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361453.3:c.266C>A	ENSP00000355046.4:p.Thr89Asn