{{Rsnum
|rsid=41407250
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBA2
|position=176765
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=41407250
|variant=0055
}}
{{omim
|id=141850
|rsnum=41407250
|variant=0011
}}{{ClinVar
|rsid=41407250
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=226764
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000017051.1; RCV000017052.1; RCV000017053.1; RCV000017054.1; RCV000017055.1
|CLNDBN=HEMOGLOBIN I; HEMOGLOBIN I (BURLINGTON); HEMOGLOBIN I (PHILADELPHIA); HEMOGLOBIN I (SKAMANIA); HEMOGLOBIN I (TEXAS)
|CLNHGVS=NC_000016.9:g.226764A>G
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=19; 141800.0055
|Disease=HEMOGLOBIN I; HEMOGLOBIN I (BURLINGTON); HEMOGLOBIN I (PHILADELPHIA); HEMOGLOBIN I (SKAMANIA); HEMOGLOBIN I (TEXAS)
}}{{PMID Auto
|PMID=740406
|Title=Hb I alpha16 Lys leads to Glu and Hb Broussais alpha90 Lys leads to Asn in Australian families.
}}

{{PMID Auto
|PMID=5480848
|Title=Diminished synthesis of an alpha chain mutant, hemoglobin I (alpha-16 lys leads to glu).
|OA=1
}}

{{PMID Auto
|PMID=5886214
|Title=Abnormal haemoglobins and the genetic code.
}}

{{PMID Auto
|PMID=6129205
|Title=Hemoglobin I (alpha 16(A14) Lys replaced by Glu) and hemoglobin J Iran (beta 77(EF1) His replaced by Asp) discovered in Japanese.
}}

{{PMID Auto
|PMID=6505702
|Title=Hemoglobin I mutation encoded at both alpha-globin loci on the same chromosome: concerted evolution in the human genome.
}}

{{PMID Auto
|PMID=7803274
|Title=The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotes.
}}