{{Rsnum
|rsid=41397847
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBA2
|position=173548
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=41397847
|variant=0005
}}
{{omim
|id=141850
|rsnum=41397847
|variant=0067
}}{{ClinVar
|rsid=41397847
|Reversed=0
|FwdREF=T
|FwdALT=A,C,G
|REF=T
|ALT=A,C,G
|RSPOS=223547
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=0
|VC=SNV
|CLNALLE=2; 3
|CLNHGVS=NC_000016.9:g.223547T>C; NC_000016.9:g.223547T>G
|CLNORIGIN=1
|CLNSRCID=
141850.0005; 141850.0067
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016897.1; RCV000016981.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=Hemoglobin Quong Sze; HEMOGLOBIN PLASENCIA
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0164294:43687002
|CLNSRC=OMIM Allelic Variant
|Disease=Hemoglobin Quong Sze; HEMOGLOBIN PLASENCIA
}}{{PMID Auto
|PMID=1726096
|Title=Detection of the Hb Quong Sze mutation in a Chinese family by selective amplification of the alpha 2-globin gene and restriction map analysis with Msp I.
}}

{{PMID Auto
|PMID=6826718
|Title=alpha-Thalassemia caused by an unstable alpha-globin mutant.
|OA=1
}}

{{PMID Auto
|PMID=7070526
|Title=Globin structural mutant alpha 125Leu leads to Pro is a novel cause of alpha-thalassaemia.
}}

{{PMID Auto
|PMID=7515267
|Title=Alpha and beta thalassaemia among Chinese children in Guangxi Province, P.R. China: molecular and haematological characterization.
}}

{{PMID Auto
|PMID=15921163
|Title=A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2).
}}

{{PMID Auto
|PMID=21077766
|Title=A dyserythropoietic anemia associated with homozygous Hb Plasencia [alpha125(H8)Leu-->Arg (alpha2)] (HBA2:c.377T>G), a variant with an unstable alpha chain.
}}

{{PMID Auto
|PMID=20854117
|Title=Hb St. Truiden [alpha68(E17)Asn-->His] and Hb Westeinde [alpha125(H8)Leu-->Gln]: two new abnormalities of the alpha2-globin gene.
}}