Canonical Allele Identifier: CA414803156
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693180
ClinVar RCV Id: RCV000854533
dbSNP Id: rs386829082
MyVariant Identifiers: chrMT:g.9531A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9531A>G , J01415.2:m.9531A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.325A>G ENSP00000354982.2:p.Thr109Ala