Canonical Allele Identifier: CA414803239
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693183
ClinVar RCV Id: RCV000854536
dbSNP Id: rs1603222374
MyVariant Identifiers: chrMT:g.9571C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9571C>T , J01415.2:m.9571C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.365C>T ENSP00000354982.2:p.Thr122Ile