{{Rsnum
|rsid=33955330
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBG1
|position=5254665
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=33955330
|variant=0007
}}{{ClinVar
|ALT=G,T
|CHROM=11
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5275895C>G
|CLNORIGIN=1
|CLNSIG=255
|FwdALT=A,C
|FwdREF=G
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=C
|RSPOS=5275895
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=33955330
|CLNACC=RCV000016103.1
|CLNDBN=HEMOGLOBIN F (FUCHU)
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=587; 142250.0007
|Disease=HEMOGLOBIN F (FUCHU)
}}{{PMID Auto
|PMID=2420697
|Title=Fetal hemoglobin variants in 80,000 Japanese neonates: high prevalence of Hb F Yamaguchi (A gamma T 80 Asp----Asn).
}}

{{PMID Auto
|PMID=8144355
|Title=Hb F-Saskatoon or alpha 2G gamma (2)21(B3)Glu-->Lys observed in a North American Indian newborn.
}}