{{Rsnum
|rsid=33984863
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBB
|position=5225633
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33984863
|variant=0501
}}{{ClinVar
|rsid=33984863
|Reversed=1
|FwdREF=G
|FwdALT=A,C,T
|REF=C
|ALT=A,G,T
|RSPOS=5246863
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000a01000002110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=1
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000011.9:g.5246863C>A; NC_000011.9:g.5246863C>G; NC_000011.9:g.5246863C>T
|CLNORIGIN=1
|CLNSIG=1
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM;NOV
}}{{PMID Auto
|PMID=20353351
|Title=Hb Perpignan [beta136(H14)Gly-->Ser], a silent variant associated with normal hematology.
}}

{{PMID Auto
|PMID=11570727
|Title=Hb 't Lange Land [beta136(H14)Gly --> Arg]: a new hemoglobin variant described in a Dutch patient of Chinese origin.
}}