{{Rsnum
|rsid=34533941
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TG)
|geno3=(TG;TG)
|Gene=HBB
|position=5226608
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34533941
|variant=0505
}}

{{ClinVar
|rsid=34533941
|Reversed=1
|FwdALT=TG
|REF=T
|ALT=TCA
|RSPOS=5247838
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5247838_5247839insCA
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=881; 141900.0338
|CLNSIG=5
|CLNCUI=C0271979
|CLNDBN=beta0^ Thalassemia
|Disease=beta0^ Thalassemia
|CLNACC=RCV000016685.24
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
}}

{{PMID Auto
|PMID=2310835
|Title=A spontaneous mutation produced a novel elongated beta-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotype.
}}

{{on chip | 23andMe v3}}