Canonical Allele Identifier: CA414803643
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693221
ClinVar RCV Id: RCV000854574
dbSNP Id: rs1603222480
MyVariant Identifiers: chrMT:g.9756T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9756T>G , J01415.2:m.9756T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.550T>G ENSP00000354982.2:p.Ser184Ala