Canonical Allele Identifier: CA337099096

Gene: MT-ND4

Linked Data

• ClinVar Variation Id: 693347
• ClinVar RCV Id: RCV000854711 ; RCV001800895
• dbSNP Id: rs386829118
• MyVariant Identifiers: chrMT:g.11150G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.11150G>A , J01415.2:m.11150G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361381.2:c.391G>A	ENSP00000354961.2:p.Ala131Thr