Canonical Allele Identifier: CA16040652

Gene: MT-CO3

Linked Data

• ClinVar Variation Id: 370052
• ClinVar RCV Id: RCV000408945 ; RCV002248640
• dbSNP Id: rs1057516064
• MyVariant Identifiers: chrMT:g.9237G>A (hg38)
• PubMed: PMID:28027978

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.9237G>A , J01415.2:m.9237G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362079.2:c.31G>A	ENSP00000354982.2:p.Val11Ile