{{Rsnum
|rsid=63751148
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBG2
|position=5254366
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=63751148
|variant=0015
}}{{ClinVar
|ALT=A,T
|CHROM=11
|CLNACC=RCV000016111.1
|CLNALLE=2
|CLNDBN=HEMOGLOBIN F (MARIETTA)
|CLNHGVS=NC_000011.9:g.5275596C>T
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=HBVAR; NCBI; OMIM Allelic Variant
|CLNSRCID=608; 63751148; 142250.0015
|Disease=HEMOGLOBIN F (MARIETTA)
|FwdALT=A,T
|FwdREF=G
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=C
|RSPOS=5275596
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;HD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000402110100
|WGT=0
|dbSNPBuildID=137
|rsid=63751148
}}{{PMID Auto
|PMID=6183237
|Title=Hb F-Marietta or G gamma I 80[EF4] Asp replaced by Asn, observed in a Caucasian baby.
}}

{{PMID Auto
|PMID=19958193
|Title=Two abnormal fetal hemoglobins found in the Sardinian population: the new Hb F-Osilo [(A)gamma119(GH2)Gly-->Ser, GGC > AGC] and Hb F-Paulinia [(G)gamma80(EF4)Asp-->Tyr, GAT > TAT] already described in the Brazilian population.
}}