{{Rsnum
|rsid=33964507
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBA2
|position=176799
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33964507
|variant=0037
}}
{{omim
|id=141850
|rsnum=33964507
|variant=0009
}}{{ClinVar
|rsid=33964507
|Reversed=0
|FwdREF=A
|FwdALT=C,G,T
|REF=A
|ALT=C,G,T
|RSPOS=226798
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000016.9:g.226798A>G
|CLNORIGIN=1
|CLNSRCID=
41; 141800.0037
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017023.1; RCV000017024.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN G (FORT WORTH); HEMOGLOBIN FORT WORTH
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN G (FORT WORTH); HEMOGLOBIN FORT WORTH
}}{{PMID Auto
|PMID=3839776
|Title=Hb Fort Worth or alpha2 27(B8)Glu----Gly beta2 in a black family from Canada.
}}

{{PMID Auto
|PMID=5122655
|Title=Hb Ft. Worth: a27Glu changed to Gly(B8). A variant present in unusually low concentration.
}}

{{PMID Auto
|PMID=1268216
|Title=Haemoglobin Spanish Town alpha27 Glu replaced by Val (B8).
}}

{{PMID Auto
|PMID=2752146
|Title=Locus assignment of two alpha-globin structural mutants from the Caribbean basin: alpha Fort de France (alpha 45 Arg) and alpha Spanish Town (alpha 27 Val).
}}

{{PMID Auto
|PMID=9658939
|Title=[Abnormal hemoglobins and thalassemias in Mexico].
}}

{{PMID Auto
|PMID=12144063
|Title=Compound heterozygosity for Hb Spanish town [alpha27(B8)Glu-->Val], Hb S [beta6(A3)Glu-->Val] and the -alpha(3.7kb) thalassemia deletion.
}}

{{PMID Auto
|PMID=11482884
|Title=Rapid identification of hemoglobin variants by electrospray ionization mass spectrometry.
}}