Canonical Allele Identifier: CA10581349
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 235541
ClinVar RCV Id: RCV000224115
dbSNP Id: rs386829076
MyVariant Identifiers: chrMT:g.9368A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9368A>G , J01415.2:m.9368A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.162A>G ENSP00000354982.2:p.Ile54Met