{{Rsnum
|rsid=33925391
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBB
|position=5225662
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33925391
|variant=0018
}}
{{omim
|id=141900
|rsnum=33925391
|variant=0111
}}
{{omim
|id=141900
|rsnum=33925391
|variant=0393
}}{{ClinVar
|rsid=33925391
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=5246892
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000011.9:g.5246892A>C; NC_000011.9:g.5246892A>G; NC_000011.9:g.5246892A>T
|CLNORIGIN=1
|CLNSIG=255
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM;NOV
|CLNACC=RCV000016741.1; RCV000016742.1; RCV000016260.1; RCV000016384.1
|CLNDBN=HEMOGLOBIN DHONBURI; HEMOGLOBIN NEAPOLIS; HEMOGLOBIN BEIRUT; HEMOGLOBIN HOFU
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0393; 141900.0018; 141900.0111
|Disease=HEMOGLOBIN DHONBURI; HEMOGLOBIN NEAPOLIS; HEMOGLOBIN BEIRUT; HEMOGLOBIN HOFU
}}{{PMID Auto
|PMID=457425
|Title=Hemoglobin Hofu (beta 126 Val is replaced by Glu) in a black American.
}}

{{PMID Auto
|PMID=750554
|Title=Hemoglobin Hofu or alpha 2 beta 2 [126 (H4) Va1 leads to Glu] found in combination with hemoglobin S.
}}

{{PMID Auto
|PMID=3923770
|Title=Hemoglobin Hofu associated with beta 0-thalassemia.
}}

{{PMID Auto
|PMID=8537236
|Title=Beta-thalassemia intermedia in an Indian female with the Hb Hofu [beta 126(H4)Val-->Glu]-beta zero-thalassemia [codons 8/9 (+G)] combination.
}}

{{PMID Auto
|PMID=6879184
|Title=Angiotensin synthesis in the brain and increased turnover in hypertensive rats.
}}

{{PMID Auto
|PMID=1463768
|Title=Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.
}}

{{PMID Auto
|PMID=1954392
|Title=Hemoglobin Neapolis, beta 126(H4)Val----Gly: a novel beta-chain variant associated with a mild beta-thalassemia phenotype and displaying anomalous stability features.
}}

{{PMID Auto
|PMID=2399911
|Title=Hemoglobin Dhonburi alpha 2 beta 2 126 (H4) Val----Gly: a new unstable beta variant producing a beta-thalassemia intermedia phenotype in association with beta zero-thalassemia.
}}

{{PMID Auto
|PMID=9028819
|Title=Compound heterozygosity for Hb Lepore-Boston and Hb Neapolis (Dhonburi) [beta 126(H4)Val-->Gly] in a patient from Naples, Italy.
}}