{{Rsnum
|rsid=41328049
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA2
|position=173207
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=41328049
|variant=0065
}}{{ClinVar
|rsid=41328049
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=223206
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050368000a01000002110100
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000016.9:g.223206G>A; NC_000016.9:g.223206G>C
|CLNORIGIN=1
|CLNSIG=1
|CLNCUI=
|Tags=PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM
}}{{PMID Auto
|PMID=15658192
|Title=A new highly unstable alpha chain variant causing alpha(+)-thalassemia: Hb Zurich Albisrieden [alpha59(E8)Gly-->Arg (alpha2)].
}}