Canonical Allele Identifier: CA414821017

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693669
• ClinVar RCV Id: RCV000855049
• dbSNP Id: rs1603224535
• MyVariant Identifiers: chrMT:g.14122A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14122A>G , J01415.2:m.14122A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.1786A>G	ENSP00000354813.2:p.Ile596Val