m.8851T>C
Resolving variant against ClinVar, gnomAD and Ensembl…
Resolving variant against ClinVar, gnomAD and Ensembl…
Tap or hover a gene, landmark or tick; genes open their page, ticks their variant.
m.8831–8871 of the revised Cambridge Reference Sequence (NC_012920.1); the boxed base is m.8851 T→C.
37 genes from Ensembl (rCRS numbering, matched to MITOMAP’s Gene Loci); landmarks and disease alleles from MITOMAP (CC BY 3.0). Circular layout after MitoWheel.