{{Rsnum
|rsid=34019507
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HBG2
|position=5254409
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=34019507
|variant=0005
}}{{ClinVar
|ALT=A,G
|CHROM=11
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5275639C>G
|CLNORIGIN=1
|CLNSIG=255
|FwdALT=C,T
|FwdREF=G
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=C
|RSPOS=5275639
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=34019507
|CLNACC=RCV000016101.1
|CLNDBN=HEMOGLOBIN F (CLARKE)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142250.0005
|Disease=HEMOGLOBIN F (CLARKE)
}}{{PMID Auto
|PMID=2442123
|Title=Hb F-Clarke or alpha 2G gamma 2(65)(E9)Lys----Asn.
}}