{{Rsnum
|rsid=34165323
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226693
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34165323
|variant=0116
}}

{{ClinVar
|rsid=34165323
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=5247923
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5247923T>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016390.1; RCV000016391.1
|CLNDBN=HEMOGLOBIN I (TOULOUSE); HEMOGLOBIN TOULOUSE
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0116
|Disease=HEMOGLOBIN I (TOULOUSE); HEMOGLOBIN TOULOUSE
}}

{{PMID Auto
|PMID=5577462
|Title=Hemoglobin toulouse alpha 2 beta 2 66 (E 10) LysGlu. Structure and consequences in molecular pathology.
}}

{{PMID Auto
|PMID=5791730
|Title=Haemoglobin I toulouse: beta-66 (E 10) lys glu: a new abnormal haemoglobin with a mutation localized on the E 10 porphyrin surrounding zone.
}}

{{PMID Auto
|PMID=7928379
|Title=Hb I-Toulouse [beta 66(E10)Lys->Glu] in association with alpha-thalassemia.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}