{{Rsnum
|rsid=34823698
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBA2
|position=177038
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=34823698
|variant=0154
}}{{ClinVar
|rsid=34823698
|Reversed=0
|FwdREF=A
|FwdALT=C,G,T
|REF=A
|ALT=C,G,T
|RSPOS=227037
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000a01000002110104
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=1
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000016.9:g.227037A>C; NC_000016.9:g.227037A>G; NC_000016.9:g.227037A>T
|CLNORIGIN=1
|CLNSIG=1
|CLNCUI=
|Tags=PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM;NOV
}}{{PMID Auto
|PMID=5416123
|Title=Studies on the function of abnormal hemoglobins. II. Oxygen equilibrium of abnormal hemoglobins: Shimonoseki, Ube II, Hikari, Gifu, and Agenogi.
}}

{{PMID Auto
|PMID=6035181
|Title=Amino acid substitution of hemoglobin Ube 2 (alpha-2 68asp beta-2): an example of successful application of partial hydrolysis of peptide with 5 per cent acetic acid.
}}

{{PMID Auto
|PMID=11939522
|Title=Hb Ube-2 in a Taiwanese subject: an A-->G substitution at codon 68 of the alpha2-globin gene.
}}

{{PMID Auto
|PMID=18473246
|Title=Hb Jeddah [alpha68(E17)Asn-->His (alpha1)]: a newly recognized alpha chain variant, seen in combination with Hb S [beta6(A3)Glu-->Val], and found in three separate families of middle eastern origin.
}}