{{Rsnum
|rsid=33985510
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5226596
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33985510
|variant=0068
}}
{{omim
|id=141900
|rsnum=33985510
|variant=0201
}}{{ClinVar
|rsid=33985510
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=5247826
|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
|CLNHGVS=NC_000011.9:g.5247826A>C; NC_000011.9:g.5247826A>G
|CLNORIGIN=1
|CLNSRCID=
449; 141900.0201; 450; 141900.0068
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016523.1; RCV000016326.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN NOTTINGHAM; HEMOGLOBIN DJELFA
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN NOTTINGHAM; HEMOGLOBIN DJELFA
}}{{PMID Auto
|PMID=701088
|Title=Hb Nottingham (alpha2beta2 (FG5) 98 val leads to gly) in a Caucasian male: clinical and biosynthetic studies.
}}

{{PMID Auto
|PMID=1634365
|Title=Hb Nottingham or alpha 2 beta 2(98)(FG5)Val----Gly observed as a de novo mutation in a Canadian child.
}}

{{PMID Auto
|PMID=13850
|Title=Hemoglobin Djelfa beta98 (FG 5) Val leads to Ala: isolation and functional properties of the heme saturated form.
}}

{{PMID Auto
|PMID=1225587
|Title=A new unstable hemoglobin mutated in beta 98 (FG 5) Val leads to Ala: hb Djelfa.
}}

{{PMID Auto
|PMID=2737917
|Title=Two rare unstable beta chain variants, Hb Mozhaisk or alpha 2 beta 292(F8)His----Arg and Hb Djelfa or alpha 2 beta 298(Fg5)Val----Ala, each being observed for the second time.
}}