{{Rsnum
|rsid=34263826
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBG1
|position=5254712
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142200
|rsnum=34263826
|variant=0014
}}
{{omim
|id=142250
|rsnum=34263826
|variant=0016
}}

{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000016112.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN F (MEINOHAMA)
|CLNHGVS=NC_000011.9:g.5275942T>C
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=581; 142250.0016
|Disease=HEMOGLOBIN F (MEINOHAMA)
|FwdALT=G
|FwdREF=A
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=T
|RSPOS=5275942
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=34263826
}}

{{PMID Auto
|PMID=6172403
|Title=Hb F-Meinohama or alpha 2 gamma 2 (5 Glu replaced by Gly; 75 Ile; 136 Gly).
}}

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