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Di laman Talasemia:
"Rantai β-globin dikodkan oleh gen tunggal pada kromosom 11; Rantai α-globin dikodkan oleh dua gen yang berkait rapat pada kromosom 16.[2] Oleh itu, dalam orang biasa dengan dua salinan setiap kromosom, dua lokus mengekod rantai β, dan empat lokus mengekod rantai α. Penghapusan salah satu lokus α mempunyai kelaziman yang tinggi pada orang keturunan Afrika atau Asia, menjadikan mereka lebih berkemungkinan menghidapi talasemia α. Talasemia β bukan sahaja biasa berlaku di Afrika, tetapi juga di Yunani dan Turki.[perlu rujukan]
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