{{Rsnum
|rsid=34647752
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBG1
|position=5248439
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG1
}}{{omim
|id=142200
|rsnum=34647752
|variant=0019
}}
{{omim
|id=142250
|rsnum=34647752
|variant=0004
}}{{ClinVar
|rsid=34647752
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=5269669
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBG1:3047
|GENE_NAME=HBG1
|GENE_ID=3047
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5269669C>T
|CLNORIGIN=1
|CLNSRCID=
142200.0019
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016163.1; RCV000016164.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN F (SIENA); HEMOGLOBIN F (HULL)
|CLNSRC=OMIM Allelic Variant
|Disease=HEMOGLOBIN F (SIENA); HEMOGLOBIN F (HULL)
}}

{{PMID Auto
|PMID=2412617
|Title=Fetal hemoglobin variants identified in adults through restriction endonuclease gene mapping methodology.
}}

{{PMID Auto
|PMID=4710228
|Title=Further characterization of haemoglobin F Hull 121 glutamic acid leads to lysine; 136 alanine.
}}

{{PMID Auto
|PMID=6038320
|Title=Haemoglobin F Hull (gamma-121 glutamic acid--lysine), homologous with haemoglobins O Arab and O Indonesia.
|OA=1
}}

{{on chip | 23andMe v4}}