The concept of random coordination ratios, RCRs, is advanced for lanthanide complexes. RCRs describe the relative probabilities of occurrence of subsets of stereoisomers of same-symmetry point groups in the limiting situation when energetic effects are equivalent. We then introduce a method to uniquely identify the stereoisomer of the coordination polyhedron of a given crystallographic structure and introduce a notation that fully characterizes its stereochemistry in an unambiguous manner, from which absolute configuration naturally follows. De facto, the coordination chirality in lanthanide complexes is a frequently overlooked property, even though these compounds often exhibit, when luminescent, high dissymmetry factors. With our methodology, we even managed to recognize a known dilanthanide complex as a meso compound, with both metal ions functioning as stereogenic centers. To achieve these results, we enumerate all possible stereoisomers of lanthanide complexes with coordination numbers from 4 to 9 for all combinations of monodentate, symmetric and asymmetric bidentate ligands, and for several shapes of coordination polyhedra. We confirmed the number of stereoisomers for each case by means of Polya's theorem. We further classified all stereoisomers according to their symmetry point groups and generated their Cartesian coordinates. This collection of all coordination polyhedra stereoisomer geometries, which is made available in the Supporting Information, can also be used to easily build starting-point geometries for theoretical calculations of metal complexes.