{{Rsnum
|rsid=33959340
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBB
|position=5226609
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33959340
|variant=0016
}}
{{omim
|id=141900
|rsnum=33959340
|variant=0035
}}
{{omim
|id=141900
|rsnum=33959340
|variant=0535
}}{{ClinVar
|rsid=33959340
|Reversed=1
|FwdREF=G
|FwdALT=A,C,T
|REF=C
|ALT=A,G,T
|RSPOS=5247839
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000011.9:g.5247839C>A; NC_000011.9:g.5247839C>G; NC_000011.9:g.5247839C>T
|CLNORIGIN=1
|CLNSRCID=
1225; 141900.0535; 436; 141900.0016; 437; 141900.0035
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016887.1; RCV000016258.1; RCV000016281.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN GELDROP ST. ANNA; HEMOGLOBIN BARCELONA; HEMOGLOBIN BUNBURY
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN GELDROP ST. ANNA; HEMOGLOBIN BARCELONA; HEMOGLOBIN BUNBURY
}}{{PMID Auto
|PMID=6842599
|Title=Structure and function of haemoglobin Barcelona Asp FG1(94) beta leads to His.
}}

{{PMID Auto
|PMID=7097767
|Title=Structural and functional studies of hemoglobin Barcelona (alpha 2 beta 2 94 Asp (FG1) replaced by His). Consequences of altering an important intrachain salt bridge involved in the alkaline Bohr effect.
}}

{{PMID Auto
|PMID=1517105
|Title=Erythrocytosis secondary to HB Bunbury [alpha 2 beta (2)94(FG1)Asp----Asn].
}}

{{PMID Auto
|PMID=6629823
|Title=A new hemoglobin with high oxygen affinity--hemoglobin bunbury: alpha 2 beta 2 [94 (FG1) Asp replaced by Asn].
}}

{{PMID Auto
|PMID=15921163
|Title=A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2).
}}