{{Rsnum
|rsid=33992775
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBG1
|position=5249767
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG1
}}{{omim
|id=142200
|rsnum=33992775
|variant=0005
}}
{{omim
|id=142250
|rsnum=33992775
|variant=0008
}}{{ClinVar
|rsid=33992775
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=5270997
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBG1:3047
|GENE_NAME=HBG1
|GENE_ID=3047
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5270997G>C
|CLNORIGIN=1
|CLNSRCID=
623; 142200.0005
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016149.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN F (CALLUNA)
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN F (CALLUNA)
}}{{PMID Auto
|PMID=6199326
|Title=Hb F-Calluna or alpha 2 gamma 2(12 Thr replaced by Arg; 75Ile; 136Ala) in a Caucasian baby.
}}

{{PMID Auto
|PMID=5763628
|Title=On the chemical abnormality of Hb "Alexandra", a fetal hemoglobin variant.
}}

{{PMID Auto
|PMID=13622677
|Title=New variant of human foetal haemoglobin.
}}