{{Rsnum
|rsid=35816645
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA1
|position=176762
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=35816645
|variant=0114
}}{{ClinVar
|rsid=35816645
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=226761
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000a01000002110100
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000016.9:g.226761G>C; NC_000016.9:g.226761G>T
|CLNORIGIN=1
|CLNSIG=1
|Tags=PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM
}}{{PMID Auto
|PMID=4135957
|Title=Hemoglobin Siam (alpha 2 15 arg beta 2): a new alpha-chain variant.
}}

{{PMID Auto
|PMID=11939517
|Title=Hb Siam [alpha15(A13)Gly-->Arg (alpha1) (GGT-->CGT)] is a typical alpha chain hemoglobinopathy without an alpha-thalassemic effect.
}}