Canonical Allele Identifier: CA414819617

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693614
• ClinVar RCV Id: RCV000854992
• dbSNP Id: rs1603224361
• MyVariant Identifiers: chrMT:g.13810G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.13810G>A , J01415.2:m.13810G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.1474G>A	ENSP00000354813.2:p.Ala492Thr