I believe the correct answer is the first option: Both parents must have the hemophilia allele.
Hemophilia is an X-linked recessive disease, which means that hemophilia is transmitted through the X sex chromosome. The female child gets an X chromosome from her mother and an X chromosome from her father. The X chromosome from her mother is dominant and If we suppose that mother has the gene for normal blood clotting and the X chromosome from her father has the gene for hemophilia, the female child won’t have hemophilia, but will be a carrier, which means that her children will have 50% chances of inheriting hemophilia. Since females have XX chromosomes, to have hemophilia manifested, both parents must have hemophilia.