{{Rsnum
|rsid=33987053
|Chromosome=16
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HBA2
|position=173520
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33987053
|variant=0110
}}
{{omim
|id=141800
|rsnum=33987053
|variant=0113
}}
{{omim
|id=141850
|rsnum=33987053
|variant=0021
}}{{ClinVar
|rsid=33987053
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=223519
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=0
|VC=SNV
|CLNALLE=3
|CLNHGVS=NC_000016.9:g.223519G>T
|CLNORIGIN=1
|CLNSRCID=
1069; 141850.0021
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000016930.25
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=alpha Thalassemia
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:NBK1435:C0002312:604131:846:68913001
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=alpha Thalassemia
}}{{PMID Auto
|PMID=6129203
|Title=Hemoglobin Oleander [alpha 116(GH4)Glu replaced by Gln beta 2]: structural and functional characterization.
}}

{{PMID Auto
|PMID=3597771
|Title=Molecular basis for nondeletion alpha-thalassemia in American blacks. Alpha 2(116GAG----UAG).
|OA=1
}}