Canonical Allele Identifier: CA414818977

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693589
• ClinVar RCV Id: RCV000854966
• dbSNP Id: rs1603224295
• MyVariant Identifiers: chrMT:g.13664T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.13664T>C , J01415.2:m.13664T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.1328T>C	ENSP00000354813.2:p.Ile443Thr