Canonical Allele Identifier: CA414807405

Gene: MT-ND4

Linked Data

• ClinVar Variation Id: 693322
• ClinVar RCV Id: RCV000854684
• dbSNP Id: rs1603223008
• MyVariant Identifiers: chrMT:g.10895A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.10895A>G , J01415.2:m.10895A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361381.2:c.136A>G	ENSP00000354961.2:p.Asn46Asp