{{Rsnum
|rsid=1135071
|Gene=HBB
|Chromosome=11
|position=5226799
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=1135071
|variant=0278
}}{{ClinVar
|rsid=1135071
|Reversed=1
|FwdREF=G
|FwdALT=C,T
|REF=C
|ALT=A,G
|RSPOS=5248029
|CHROM=11
|GMAF=0.0005
|dbSNPBuildID=86
|SSR=0
|SAO=1
|VP=0x050368000000000116110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248029C>A
|CLNORIGIN=1
|CLNSIG=255
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591; .
|COMMON=0
|CLNACC=RCV000016619.1; RCV000016620.24
|CLNDBN=HEMOGLOBIN TACOMA; Heinz body hemolytic anemia
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0278
|Disease=HEMOGLOBIN TACOMA; Heinz body hemolytic anemia
}}{{PMID Auto
|PMID=5785231
|Title=Structural characterization of hemoglobin Tacoma.
}}

{{PMID Auto
|PMID=5869485
|Title=Hemoglobin tacoma--a beta-chain variant associated with increased hb A2.
}}

{{PMID Auto
|PMID=8226093
|Title=Rare beta chain hemoglobin variants found in Swedish patients during HBA1c analysis.
}}

{{PMID Auto
|PMID=9140720
|Title=A significant beta-thalassemia heterogeneity in the United Arab Emirates.
}}