m.9029A>G
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.9009–9049 of the revised Cambridge Reference Sequence (NC_012920.1); the boxed base is m.9029 A→G.
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.