{{Rsnum
|rsid=33947020
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HBB
|position=5225683
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33947020
|variant=0026
}}
{{omim
|id=141900
|rsnum=33947020
|variant=0394
}}{{ClinVar
|rsid=33947020
|Reversed=1
|FwdREF=G
|FwdALT=A,C,T
|REF=C
|ALT=A,G,T
|RSPOS=5246913
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000011.9:g.5246913C>A; NC_000011.9:g.5246913C>G; NC_000011.9:g.5246913C>T
|CLNORIGIN=1
|CLNSRCID=
503; 141900.0026; 504; 141900.0394; 141900.0075; 141900.0172
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016263.1; RCV000016743.1; RCV000016336.1; RCV000016486.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN BOUGARDIREY-MALI; HEMOGLOBIN IOWA; HEMOGLOBIN FANNIN-LUBBOCK; HEMOGLOBIN MASUDA
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN BOUGARDIREY-MALI; HEMOGLOBIN IOWA; HEMOGLOBIN FANNIN-LUBBOCK; HEMOGLOBIN MASUDA
}}{{PMID Auto
|PMID=500370
|Title=Hemoglobin Bougardirey-Mali beta 119 (GH2) Gly replaced by Val. An electrophoretically silent variant migrating in isoelectrofocusing as Hb F.
}}

{{PMID Auto
|PMID=15008260
|Title=Diagnosis and characterization of Hb C/Hb Iowa: a rare but easily misidentified compound heterozygous condition.
}}

{{PMID Auto
|PMID=15481899
|Title=DNA sequence of Hb Iowa.
}}