{{Rsnum
|rsid=34997902
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBG2
|position=5253344
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=34997902
|variant=0021
}}

{{ClinVar
|ALT=A,G
|CHROM=11
|CLNACC=RCV000016117.1
|CLNALLE=2
|CLNDBN=HEMOGLOBIN F (PORT ROYAL)
|CLNHGVS=NC_000011.9:g.5274574T>G
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=616; 142250.0021
|Disease=HEMOGLOBIN F (PORT ROYAL)
|FwdALT=C,T
|FwdREF=A
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=T
|RSPOS=5274574
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;HD;GNO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000502110100
|WGT=0
|dbSNPBuildID=126
|rsid=34997902
}}

{{PMID Auto
|PMID=4846278
|Title=Haemoglobin F Port Royal (alpha2G gamma2 125 Glu leads to Ala).
}}

{{on chip | 23andMe v2}}
{{on chip | Illumina Human 1M}}