{{Rsnum
|rsid=33954632
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBB
|position=5226939
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33954632
|variant=0094
}}
{{omim
|id=141900
|rsnum=33954632
|variant=0295
}}

{{ClinVar
|rsid=33954632
|Reversed=1
|FwdREF=C
|FwdALT=A,G,T
|REF=G
|ALT=A,C,T
|RSPOS=5248169
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000402110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 3
|CLNHGVS=NC_000011.9:g.5248169G>A; NC_000011.9:g.5248169G>T
|CLNORIGIN=1
|CLNSRCID=
282; 141900.0094; 280; 141900.0295
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016364.1; RCV000016638.1; RCV000016639.1
|Tags=RV;PM;PMC;S3D;SLO;HD;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN GRANGE-BLANCHE; HEMOGLOBIN VOLGA; HEMOGLOBIN DRENTHE
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN GRANGE-BLANCHE; HEMOGLOBIN VOLGA; HEMOGLOBIN DRENTHE
}}

{{PMID Auto
|PMID=952960
|Title=Hb-Volga or alpha 2 beta 2 27(B9)Ala replaced by Asp. An unstable hemoglobin variant in three generations of a Dutch family.
}}

{{PMID Auto
|PMID=1225571
|Title=Haemoglobin Volga, beta27, (B9) Ala leads to Asp, a new highly unstable haemoglobin with a suppressed charge.
}}

{{PMID Auto
|PMID=3666141
|Title=Hemoglobin Grange-Blanche [beta 27(B9) Ala----Val], a new variant with normal expression and increased affinity for oxygen.
}}

{{PMID Auto
|PMID=9415844
|Title=Hb Siirt [beta 27(B9)Ala-->Gly]: a new, electrophoretically silent, hemoglobin variant.
}}

{{on chip | HumanOmni1Quad}}