{{Rsnum
|rsid=33970907
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBG1
|position=5249737
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG1
}}{{omim
|id=142200
|rsnum=33970907
|variant=0015
}}
{{omim
|id=142250
|rsnum=33970907
|variant=0024
}}
{{omim
|id=142250
|rsnum=33970907
|variant=0029
}}{{ClinVar
|rsid=33970907
|Reversed=1
|FwdREF=A
|FwdALT=G,T
|REF=T
|ALT=A,C
|RSPOS=5270967
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBG1:3047
|GENE_NAME=HBG1
|GENE_ID=3047
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5270967T>C
|CLNORIGIN=1
|CLNSRCID=
624; 142200.0015
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016159.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN F (KUALA LUMPUR)
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN F (KUALA LUMPUR)
}}{{PMID Auto
|PMID=4765089
|Title=Structural identification of haemoglobin F Kuala Lumpur: alpha2 gamma2 22(B4)Asp leads to Gly; 136 Ala.
}}