The trick with translocation questions is to anchor on the driver gene. For Burkitt lymphoma that gene is MYC, which sits on chromosome 8. Putting MYC under the control of a strongly active immunoglobulin promoter switches it on permanently and drives the very high proliferation that defines this tumour.
The commonest way this happens is a swap between chromosome 8 and chromosome 14, where the immunoglobulin heavy-chain gene lives. That gives t(8;14), the signature of Burkitt lymphoma.
The remaining choices belong to other malignancies. The cyclin D1 rearrangement t(11;14) marks mantle cell lymphoma. The t(15;17) fusion that joins PML and RARA defines acute promyelocytic leukemia. The BCL2 rearrangement t(14;18) is the marker of follicular lymphoma. None of these is the MYC translocation.
So the correct association for Burkitt lymphoma is t(8;14).
\[\boxed{\text{t(8;14) (option A)}}\]