m.11778G>A
Resolving variant against ClinVar, gnomAD and Ensembl…
Resolving variant against ClinVar, gnomAD and Ensembl…
gnomad: gnomAD lookup failed: Error: gnomAD API error: 400
Tap or hover a gene, landmark or tick; genes open their page, ticks their variant.
m.11758–11798 of the revised Cambridge Reference Sequence (NC_012920.1); the boxed base is m.11778 G→A.
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.