Canonical Allele Identifier: CA337097398
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692649
ClinVar RCV Id: RCV000853971
dbSNP Id: rs879164161
MyVariant Identifiers: chrMT:g.6445C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6445C>T , J01415.2:m.6445C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.542C>T ENSP00000354499.2:p.Thr181Met