{{Rsnum
|rsid=34150306
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBG2
|position=5254374
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=34150306
|variant=0009
}}

{{ClinVar
|ALT=A,C
|CHROM=11
|CLNACC=RCV000016105.1
|CLNALLE=2
|CLNDBN=HEMOGLOBIN F (KENNESTONE)
|CLNHGVS=NC_000011.9:g.5275604T>C
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=607; 142250.0009
|Disease=HEMOGLOBIN F (KENNESTONE)
|FwdALT=G,T
|FwdREF=A
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=T
|RSPOS=5275604
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;HD;GNO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000502110100
|WGT=0
|dbSNPBuildID=126
|rsid=34150306
}}

{{PMID Auto
|PMID=6192110
|Title=Hb F-Kennestone or alpha 2G gamma 2 (EF1)77 His leads to Arg observed in a Caucasian baby.
}}

{{on chip | 23andMe v2}}
{{on chip | Illumina Human 1M}}