Canonical Allele Identifier: CA414802445
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693127
ClinVar RCV Id: RCV000854478
dbSNP Id: rs1556423637
MyVariant Identifiers: chrMT:g.9214A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9214A>G , J01415.2:m.9214A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.8A>G ENSP00000354982.2:p.His3Arg