{{Rsnum
|rsid=76728603
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBB
|position=5226774
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=11549407
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=76728603
|variant=0004
}}
{{omim
|id=141900
|rsnum=76728603
|variant=0290
}}
{{omim
|id=141900
|rsnum=76728603
|variant=0312
}}{{PMID Auto
|PMID=1115799
|Title=Two new hemoglobins. Hemoglobin Alabama (beta39(C5)Gln leads to Lys) and hemoglobin Montgomery (alpha 48(CD 6) Leu leads to Arg).
}}

{{PMID Auto
|PMID=893132
|Title=Hb Vaasa or alpha2beta2 (39(C5)Gln replaced by Glu), a mildly unstable variant found in a Finnish family.
}}

{{PMID Auto
|PMID=2200760
|Title=Beta-thalassemia in Turkey.
}}

{{PMID Auto
|PMID=6457059
|Title=beta zero thalassemia in Sardinia is caused by a nonsense mutation.
|OA=1
}}

{{PMID Auto
|PMID=6985481
|Title=Nonsense and frameshift mutations in beta 0-thalassemia detected in cloned beta-globin genes.
}}