{{Rsnum
|rsid=63751150
|Chromosome=16
|Orientation=plus
|geno1=(-;-)
|geno2=(-;ACC)
|geno3=(ACC;ACC)
|Gene=HBA2
|position=176951
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=63751150
|variant=0184
}}{{ClinVar
|ALT=C
|CHROM=16
|CLNACC=RCV000017204.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN TAYBE
|CLNHGVS=NC_000016.9:g.226950_226952delACC
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141800.0184
|Disease=HEMOGLOBIN TAYBE
|FwdREF=ACC
|GENEINFO=HBA1:3039
|GENE_ID=3039
|GENE_NAME=HBA1
|REF=CACC
|RSPOS=226946
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=63751150
}}{{PMID Auto
|PMID=7942784
|Title=Compound heterozygosity for two alpha-globin gene defects, Hb Taybe (alpha 1; 38 or 39 minus Thr) and a poly A mutation (alpha 2; AATAAA-->AATAAG), results in a severe hemolytic anemia.
}}

{{PMID Auto
|PMID=7994622
|Title=Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygous.
}}

{{PMID Auto
|PMID=9576334
|Title=HB Taybe: description of genetics and laboratory findings in an Israeli Arab family.
}}