{{Rsnum
|rsid=63750294
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA1
|position=172967
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141800
|rsnum=63750294
|variant=0049
}}{{ClinVar
|ALT=C
|CHROM=16
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.222966G>C
|CLNORIGIN=1
|CLNSIG=1
|FwdALT=C
|FwdREF=G
|GENEINFO=HBA2:3040
|GENE_ID=3040
|GENE_NAME=HBA2
|REF=G
|RSPOS=222966
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000a01000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=63750294
}}{{PMID Auto
|PMID=852596
|Title=Haemoglobin Handsworth alpha 18 (A16) glycine leads to arginne.
}}

{{PMID Auto
|PMID=4030381
|Title=Hemoglobin Handsworth or alpha2 18(A16)Gly----Arg beta2 in a Saudi newborn.
}}

{{PMID Auto
|PMID=7216818
|Title=Hemoglobin Handsworth (gamma 18 (A16) Gly leads to Arg) in a Chinese.
}}