{{Rsnum
|rsid=33949930
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5227017
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33949930
|variant=0069
}}
{{omim
|id=141900
|rsnum=33949930
|variant=0233
}}
{{omim
|id=141900
|rsnum=33949930
|variant=0497
}}{{ClinVar
|rsid=33949930
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=5248247
|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.5248247A>C; NC_000011.9:g.5248247A>G; NC_000011.9:g.5248247A>T
|CLNORIGIN=1
|CLNSIG=255
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM;NOV
|CLNACC=RCV000016854.1; RCV000016563.1; RCV000016327.1
|CLNDBN=HEMOGLOBIN WATFORD; HEMOGLOBIN RALEIGH; HEMOGLOBIN DOHA
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0497; 141900.0233; 141900.0069
|Disease=HEMOGLOBIN WATFORD; HEMOGLOBIN RALEIGH; HEMOGLOBIN DOHA
}}{{PMID Auto
|PMID=20942
|Title=Hemoglobin Raleigh (beta1 valine replaced by acetylalanine). Structural and functional characterization.
}}

{{PMID Auto
|PMID=8226093
|Title=Rare beta chain hemoglobin variants found in Swedish patients during HBA1c analysis.
}}

{{PMID Auto
|PMID=9625056
|Title=Hemoglobin Raleigh as the cause of a falsely increased hemoglobin A1C in an automated ion-exchange HPLC method.
}}

{{PMID Auto
|PMID=3840039
|Title=Hb Doha or alpha 2 beta 2[X-N-Met-1(NA1)Val----Glu]; a new beta-chain abnormal hemoglobin observed in a Qatari female.
}}

{{PMID Auto
|PMID=11186267
|Title=Hb Watford [beta1(NA1)Val-->Gly]: a new, clinically silent hemoglobin variant in linkage with a new neutral mutation.
}}

{{PMID Auto
|PMID=11482884
|Title=Rapid identification of hemoglobin variants by electrospray ionization mass spectrometry.
}}