{{Rsnum
|rsid=35020253
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|position=5253366
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene=HBG2
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=35020253
|variant=0047
}}

{{ClinVar
|ALT=G
|CHROM=11
|CLNACC=RCV000016142.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN F (CALABRIA)
|CLNHGVS=NC_000011.9:g.5274596A>G
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=892; 142250.0047
|Disease=HEMOGLOBIN F (CALABRIA)
|FwdALT=C
|FwdREF=T
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=A
|RSPOS=5274596
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;HD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000402110100
|WGT=0
|dbSNPBuildID=126
|rsid=35020253
}}

{{PMID Auto
|PMID=10722114
|Title=A new, electrophoretically silent, fetal hemoglobin variant: Hb F-Calabria [Ggamma118(GH1)Phe-->Leu].
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}