Canonical Allele Identifier: CA337099043

Gene: MT-ND4

Linked Data

• ClinVar Variation Id: 693327
• ClinVar RCV Id: RCV000854689
• dbSNP Id: rs878931758
• MyVariant Identifiers: chrMT:g.10914G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.10914G>A , J01415.2:m.10914G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361381.2:c.155G>A	ENSP00000354961.2:p.Cys52Tyr