{{Rsnum
|rsid=33937393
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226587
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33937393
|variant=0006
}}

{{ClinVar
|rsid=33937393
|Reversed=1
|FwdREF=A
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=5247817
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000402110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5247817T>C
|CLNORIGIN=1
|CLNSIG=255
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;HD;OTHERKG;LSD;OM
|CLNACC=RCV000016247.1
|CLNDBN=HEMOGLOBIN ALBERTA
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=61; 141900.0006
|Disease=HEMOGLOBIN ALBERTA
}}

{{PMID Auto
|PMID=750556
|Title=A second patient with hemoglobin Alberta, a high-oxygen-affinity variant causing erythrocytosis and forming asymmetric tetramers.
}}

{{PMID Auto
|PMID=903694
|Title=Isoelectric focusing studies of a "stable" asymmetrical hybrid formed with a new hemoglobin variant, hemoglobin alberta (alpha2beta2101(G3)Glu leads to Gly).
}}

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

{{on chip | HumanOmni1Quad}}