Canonical Allele Identifier: CA254855

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 9699
• ClinVar RCV Id: RCV000010339
• dbSNP Id: rs267606894
• MyVariant Identifiers: chrMT:g.12770A>G (hg38)
• PubMed: PMID:12509858

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12770A>G , J01415.2:m.12770A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.434A>G	ENSP00000354813.2:p.Glu145Gly