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Table 1 The most commonly known HPFG/δβ-thalassemia and their associated phenotypes in Southern China

From: Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China

Name

Type of Thalassemia

Mutation

Phenotype

Chinese Ggamma (Agammadeltabeta)0-Thal

(Agamma-delta-beta)0

NG_000007.3:g.48795_127698del78904

Microcytic anemia (HP:0001903); Persistence of hemoglobin F (HP:0011904);

SEA-HPFH deletion

HPFH

NC_000011.9:g.5222878_5250288del27411

Microcytic anemia (HP:0001903);Persistence of hemoglobin F (HP:0011904);