{{Rsnum
|rsid=121913128
|Chromosome=16
|Orientation=plus
|geno1=(-;-)
|geno2=(-;CGT)
|geno3=(CGT;CGT)
|Gene=HBA1
|position=177406
|Gene_s=HBA1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=141800
|rsnum=121913128
|variant=0083
}}{{ClinVar
|rsid=121913128
|Reversed=0
|FwdREF=CGT
|FwdALT=
|REF=CCGT
|ALT=C
|RSPOS=227404
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110200
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.227405_227407delCGT
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000017081.1; RCV000017082.1
|CLNDBN=HEMOGLOBIN KOELLIKER; HEMOGLOBIN F (KOELLIKER)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141800.0083
|Disease=HEMOGLOBIN KOELLIKER; HEMOGLOBIN F (KOELLIKER)
}}