Canonical Allele Identifier: CA414817902

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693553
• ClinVar RCV Id: RCV000854928
• dbSNP Id: rs1603224181
• MyVariant Identifiers: chrMT:g.13415G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.13415G>A , J01415.2:m.13415G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.1079G>A	ENSP00000354813.2:p.Gly360Glu