{{Rsnum
|rsid=56205611
|Gene=HBG1
|Chromosome=11
|position=5248393
|Orientation=minus
|GMAF=0.004132
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=HBG1
}}{{omim
|id=142200
|rsnum=56205611
|variant=0032
}}{{ClinVar
|ALT=C
|CAF=0.9959; 0.004132
|CHROM=11
|CLNACC=RCV000016180.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN F (CHARLOTTE)
|CLNHGVS=NC_000011.9:g.5269623G>C
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142200.0032
|COMMON=1
|Disease=HEMOGLOBIN F (CHARLOTTE)
|FwdALT=G
|FwdREF=C
|GENEINFO=HBG1:3047
|GENE_ID=3047
|GENE_NAME=HBG1
|REF=G
|RSPOS=5269623
|Reversed=1
|SAO=1
|SSR=1
|Tags=RV;PM;PMC;S3D;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000016110100
|WGT=0
|dbSNPBuildID=129
|rsid=56205611
}}{{PMID Auto
|PMID=1714434
|Title=Hb F-Charlotte, an A gamma variant with a threonine residue in position gamma 75 and a glycine residue in position gamma 136.
}}