{{Rsnum
|rsid=34876238
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBG2
|position=5254303
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2,LOC100288908
}}{{omim
|id=142250
|rsnum=34876238
|variant=0011
}}

{{ClinVar
|rsid=34876238
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=5275533
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBG2:3048
|GENE_NAME=HBG2
|GENE_ID=3048
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5275533C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016107.1
|CLNDBN=HEMOGLOBIN F (LA GRANGE)
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=611; 142250.0011
|Disease=HEMOGLOBIN F (LA GRANGE)
}}

{{PMID Auto
|PMID=6206897
|Title=Hb F-La Grange or alpha 2 gamma 2 101(G3)Glu----Lys; 75Ile; 136Gly: a high oxygen affinity fetal hemoglobin variant observed in a Caucasian newborn.
}}

{{on chip | 23andMe v2}}