{{Rsnum
|rsid=33995148
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226708
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33995148
|variant=0190
}}
{{omim
|id=141900
|rsnum=33995148
|variant=0317
}}
{{omim
|id=141900
|rsnum=33995148
|variant=0514
}}{{ClinVar
|rsid=33995148
|Reversed=1
|FwdREF=A
|FwdALT=C,G,T
|REF=T
|ALT=A,C,G
|RSPOS=5247938
|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.5247938T>A; NC_000011.9:g.5247938T>C; NC_000011.9:g.5247938T>G
|CLNORIGIN=1
|CLNSRCID=
141900.0317; 353; 141900.0190; 1145; 141900.0514
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016661.21; RCV000016510.1; RCV000016870.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=beta0^ Thalassemia; HEMOGLOBIN N (SEATTLE); HEMOGLOBIN POCOS DE CALDAS
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
|CLNSRC=OMIM Allelic Variant; HBVAR
|Disease=beta0^ Thalassemia; HEMOGLOBIN N (SEATTLE); HEMOGLOBIN POCOS DE CALDAS
}}{{PMID Auto
|PMID=5637049
|Title=Structural characterization of hemoglobin-N-Seattle.
}}

{{PMID Auto
|PMID=2458145
|Title=Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States.
}}

{{PMID Auto
|PMID=12484633
|Title=A novel beta-globin variant: Hb Pocos de Caldas [beta 61(E5)Lys-->Gln].
}}