{{Rsnum
|rsid=33931779
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5226710
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33931779
|variant=0053
}}
{{omim
|id=141900
|rsnum=33931779
|variant=0321
}}{{ClinVar
|rsid=33931779
|Reversed=1
|FwdREF=T
|FwdALT=A,C
|REF=A
|ALT=G,T
|RSPOS=5247940
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.5247940A>G; NC_000011.9:g.5247940A>T
|CLNORIGIN=1
|CLNSRCID=
351; 141900.0053; 352; 141900.0321
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016304.1; RCV000016666.24; RCV000016667.1
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN COLLINGWOOD; Beta-plus-thalassemia; HEMOGLOBIN CAGLIARI
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN COLLINGWOOD; Beta-plus-thalassemia; HEMOGLOBIN CAGLIARI
}}{{PMID Auto
|PMID=6421773
|Title=Hemoglobin Collingwood beta 60 (E4) Val replaced by Ala. A new unstable hemoglobin.
}}

{{PMID Auto
|PMID=1985702
|Title=Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathy.
}}