Canonical Allele Identifier: CA414819659

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693618
• ClinVar RCV Id: RCV000854996
• dbSNP Id: rs1603224368
• MyVariant Identifiers: chrMT:g.13820T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.13820T>C , J01415.2:m.13820T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.1484T>C	ENSP00000354813.2:p.Phe495Ser