{{Rsnum
|rsid=33986902
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBA1
|position=176736
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33986902
|variant=0032
}}
{{omim
|id=141800
|rsnum=33986902
|variant=0128
}}
{{omim
|id=141800
|rsnum=33986902
|variant=0145
}}{{ClinVar
|rsid=33986902
|Reversed=0
|FwdREF=A
|FwdALT=C,G,T
|REF=A
|ALT=C,G,T
|RSPOS=226735
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000016.9:g.226735A>C; NC_000016.9:g.226735A>G; NC_000016.9:g.226735A>T
|CLNORIGIN=1
|CLNSRCID=
5; 141800.0128; 9; 141800.0145; 7; 141800.0032
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017150.1; RCV000017165.1; RCV000017019.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN SAWARA; HEMOGLOBIN SWAN RIVER; HEMOGLOBIN FERNDOWN
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN SAWARA; HEMOGLOBIN SWAN RIVER; HEMOGLOBIN FERNDOWN
}}{{PMID Auto
|PMID=20980
|Title=Increased oxygen affinity for hemoglobin Sawara: alphaA4(6) aspartic acid replaced by alanine.
}}

{{PMID Auto
|PMID=1241593
|Title=Studies of abnormal hemoglobins in western Japan. Frequency of visible hemoglobin variants, and chemical characterization of hemoglobin Sawara (alpha 26Alabeta2) and hemoglobin Mugino (Hb L Ferrara; alpha247Glybeta2).
}}

{{PMID Auto
|PMID=4744335
|Title=Hemoglobin Sawara: alpha 6(A4) aspartic acid leads to alanine.
}}

{{PMID Auto
|PMID=7238857
|Title=Haemoglobin Ferndown (alpha 6 [A4] aspartic acid replaced by valine).
}}

{{PMID Auto
|PMID=2753737
|Title=Hb Swan River [alpha 6(A4) Asp----Gly] initial identification in an Australian family.
}}

{{PMID Auto
|PMID=3583768
|Title=Hemoglobin Swan River [alpha 6(A4)Asp----Gly].
}}

{{PMID Auto
|PMID=8745434
|Title=HB Swan River [alpha 6(A4)ASP-->Gly] observed in a Japanese man.
}}