m.14596A>T
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.14576–14616 of the revised Cambridge Reference Sequence (NC_012920.1); the boxed base is m.14596 A→T.
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.