{{Rsnum
|rsid=33967755
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBB
|position=5226671
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33967755
|variant=0183
}}
{{omim
|id=141900
|rsnum=33967755
|variant=0283
}}{{ClinVar
|rsid=33967755
|Reversed=1
|FwdREF=A
|FwdALT=G,T
|REF=T
|ALT=A,C
|RSPOS=5247901
|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; 2
|CLNHGVS=NC_000011.9:g.5247901T>A; NC_000011.9:g.5247901T>C
|CLNORIGIN=1
|CLNSRCID=
384; 141900.0183; 385; 141900.0283
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016499.1; RCV000016625.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN MOBILE; HEMOGLOBIN TILBURG
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN MOBILE; HEMOGLOBIN TILBURG
}}{{PMID Auto
|PMID=1018330
|Title=Hemoglobin Vancouver [alpha2beta2(73)(E17) Asp replaced by Tyr]: its structure and function.
}}

{{PMID Auto
|PMID=1180880
|Title=Hb Mobile [alpha2beta2 73(E17)Asp replaced by Val]: a new variant.
}}

{{PMID Auto
|PMID=3191145
|Title=Hemoglobin Tilburg: alpha 2-beta 2 73 (E 17) Asp----Gly. A new hemoglobin with reduced oxygen affinity.
}}