{{Rsnum
|rsid=35672478
|Chromosome=16
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GTG)
|geno3=(GTG;GTG)
|Gene=HBA2
|position=177020
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=35672478
|variant=0202
}}

{{ClinVar
|rsid=35672478
|Reversed=0
|FwdREF=GTG
|FwdALT=
|REF=GGTG
|ALT=G
|RSPOS=227018
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.227019_227021delGTG
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=906; 141800.0202
|CLNSIG=255
|CLNCUI=CN077787
|CLNDBN=HEMOGLOBIN AGHIA SOPHIA; Hemoglobin H disease, nondeletional
|Disease=HEMOGLOBIN AGHIA SOPHIA; Hemoglobin H disease
|CLNACC=RCV000017221.1; RCV000022601.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN077787
}}

{{PMID Auto
|PMID=10569720
|Title=Hb Aghia Sophia [alpha62(E11)Val-->0 (alpha1)], an "in-frame" deletion causing alpha-thalassemia.
}}

{{on chip | 23andMe v3}}