Canonical Allele Identifier: CA10581355

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 235555
• ClinVar RCV Id: RCV000224130
• dbSNP Id: rs28359176
• MyVariant Identifiers: chrMT:g.13485A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.13485A>G , J01415.2:m.13485A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.1149A>G	ENSP00000354813.2:p.Ile383Met