{{Rsnum
|rsid=34703519
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBG2
|position=5253360
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=34703519
|variant=0003
}}{{ClinVar
|ALT=G
|CHROM=11
|CLNACC=RCV000016099.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN F (CALTECH)
|CLNHGVS=NC_000011.9:g.5274590T>G
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=614; 142250.0003
|Disease=HEMOGLOBIN F (CALTECH)
|FwdALT=C
|FwdREF=A
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=T
|RSPOS=5274590
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=34703519
}}{{PMID Auto
|PMID=6186635
|Title=Hemoglobin F-Caltech: alpha 2 G gamma 2 120Lys replaced by Gln.
}}