Canonical Allele Identifier: CA414803426
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693200
ClinVar RCV Id: RCV000854553
dbSNP Id: rs1603222423
MyVariant Identifiers: chrMT:g.9660A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9660A>G , J01415.2:m.9660A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.454A>G ENSP00000354982.2:p.Ile152Val