Canonical Allele Identifier: CA414812824

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693426
• ClinVar RCV Id: RCV000854796
• dbSNP Id: rs1603223688
• MyVariant Identifiers: chrMT:g.12362C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12362C>T , J01415.2:m.12362C>T	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.26C>T	ENSP00000354813.2:p.Thr9Ile