{{Rsnum
|rsid=33964317
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBA2
|position=176759
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33964317
|variant=0031
}}{{ClinVar
|rsid=33964317
|Reversed=0
|FwdREF=T
|FwdALT=A,C
|REF=T
|ALT=A,C
|RSPOS=226758
|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.226758T>A; NC_000016.9:g.226758T>C
|CLNORIGIN=1
|CLNSIG=1
|CLNCUI=
|Tags=PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM
}}{{PMID Auto
|PMID=6725558
|Title=Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia.
|OA=1
}}

{{PMID Auto
|PMID=6882779
|Title=Hemoglobin Evanston: alpha 14(A12) Trp leads to Arg. A variant hemoglobin associated with alpha-thalassemia-2.
}}

{{PMID Auto
|PMID=15008259
|Title=A new Hb evanston allele [alpha14(A12)Trp --> Arg] found solely, and in the presence of common alpha-thalassemia deletions, in three independent Asian cases.
}}