t(15;17)(q24;q21)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A chromosomal translocation associated with creation of a fusion between the PML and RARA genes. It is seen in variants of acute promyelocytic leukemia.

**Synonyms:** - t(15;17)(q22;q12) - t(15;17)(q22;q12) PML::RARA - t(15;17)(q22;q21) - t(15;17)(q24.1;q21.2)