{{Rsnum
|rsid=36049074
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBG2
|position=5253368
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=36049074
|variant=0014
}}{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000016110.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN F (MALTA)
|CLNHGVS=NC_000011.9:g.5274598T>C
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=613; 142250.0014
|Disease=HEMOGLOBIN F (MALTA)
|FwdALT=G
|FwdREF=A
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=T
|RSPOS=5274598
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=36049074
}}

{{PMID Auto
|PMID=588240
|Title=Detection and quantitation of the fetal hemoglobin variant Hb F-Malta-I in adults.
}}

{{PMID Auto
|PMID=1709134
|Title=The linkage of Hb Valletta [alpha 2 beta 287(f3)Thr----Pro] and Hb F-Malta-I [alpha 2G gamma 2117(G19)His----Arg] in the Maltese population.
}}

{{PMID Auto
|PMID=5792729
|Title=Haemoglobin F(Malta): a new foetal haemoglobin variant with a high incidence in Maltese infants.
}}

{{on chip | 23andMe v4}}