{{Rsnum
|rsid=33947415
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226684
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33947415
|variant=0050
}}
{{omim
|id=141900
|rsnum=33947415
|variant=0147
}}{{ClinVar
|rsid=33947415
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=5247914
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000040002110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.5247914C>G; NC_000011.9:g.5247914C>T
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=
378; 141900.0147; 377; 141900.0050
|CLNSIG=255
|CLNCUI=
|CLNDBN=HEMOGLOBIN KENITRA; HEMOGLOBIN CITY OF HOPE; Beta thalassemia intermedia
|Disease=HEMOGLOBIN KENITRA; HEMOGLOBIN CITY OF HOPE; Beta thalassemia intermedia
|CLNACC=
RCV000016437.1; RCV000016301.1; RCV000029969.1
|Tags=RV;PM;PMC;S3D;SLO;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0472767:191189009
}}{{PMID Auto
|PMID=1353069
|Title=Hb City of Hope [beta 69(E13)Gly----Ser] in Italy: association of the gene with haplotype IX.
}}

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

{{PMID Auto
|PMID=2467892
|Title=Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemia.
}}

{{PMID Auto
|PMID=3957690
|Title=The identification of five rare beta-chain abnormal hemoglobins by high performance liquid chromatographic procedures.
}}

{{PMID Auto
|PMID=6434492
|Title=A silent hemoglobin variant detected by HPLC: hemoglobin City of Hope beta 69 (E13) Gly----Ser.
}}

{{PMID Auto
|PMID=17932132
|Title=Mass spectrometry: a tool for enhanced detection of hemoglobin variants.
}}{{PMID Auto
|PMID=3838975
|Title=Hemoglobin kenitra alpha 2 beta 2 69 (E13) Gly----Arg. A new beta variant of elevated expression associated with alpha-thalassemia, found in a Moroccan woman.
}}