{{Rsnum
|rsid=33929459
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226952
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33929459
|variant=0216
}}{{ClinVar
|rsid=33929459
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=5248182
|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.5248182C>A; NC_000011.9:g.5248182C>T
|CLNORIGIN=1
|CLNSRCID=
271; 141900.0216; 141900.0244
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016544.1; RCV000016576.1
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN PALMERSTON NORTH; HEMOGLOBIN S (ANTILLES)
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN PALMERSTON NORTH; HEMOGLOBIN S (ANTILLES)
}}{{PMID Auto
|PMID=7161106
|Title=Hemoglobin Palmerston North beta 23 (B5) Val replaced by Phe. A new variant identified in a patient with polycythemia.
}}