Canonical Allele Identifier: CA414814056

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693470
• ClinVar RCV Id: RCV000854842
• dbSNP Id: rs1603223840
• MyVariant Identifiers: chrMT:g.12622G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12622G>A , J01415.2:m.12622G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.286G>A	ENSP00000354813.2:p.Val96Ile