{{Rsnum
|rsid=33936254
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBB
|position=5226954
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33936254
|variant=0061
}}
{{omim
|id=141900
|rsnum=33936254
|variant=0081
}}
{{omim
|id=141900
|rsnum=33936254
|variant=0088
}}{{ClinVar
|rsid=33936254
|Reversed=1
|FwdREF=A
|FwdALT=C,G,T
|REF=T
|ALT=A,C,G
|RSPOS=5248184
|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.5248184T>A; NC_000011.9:g.5248184T>C; NC_000011.9:g.5248184T>G
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=
268; 141900.0061; 265; 141900.0088; 266; 141900.0081
|CLNSIG=255
|CLNCUI=
|CLNDBN=HEMOGLOBIN D (GRANADA); HEMOGLOBIN G (TAIPEI); HEMOGLOBIN G (COUSHATTA); HEMOGLOBIN G (SASKATOON); HEMOGLOBIN G (HSIN-CHU); HEMOGLOBIN G (TAEGU); beta Thalassemia
|Disease=HEMOGLOBIN D (GRANADA); HEMOGLOBIN G (TAIPEI); HEMOGLOBIN G (COUSHATTA); HEMOGLOBIN G (SASKATOON); HEMOGLOBIN G (HSIN-CHU); HEMOGLOBIN G (TAEGU); beta Thalassemia
|CLNACC=
RCV000016312.1; RCV000016356.1; RCV000016343.1; RCV000016344.1; RCV000016345.1; RCV000016346.1; RCV000030001.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:C0005283:613985:848:65959000
}}{{PMID Auto
|PMID=140
|Title=Regulation and properties of an invertase from Clostridium pasteurianum.
}}

{{PMID Auto
|PMID=721611
|Title=Occurrence of hemoglobin G Coushatta in Japan.
}}

{{PMID Auto
|PMID=2265836
|Title=Abnormal hemoglobins in the Silk Road region of China.
}}

{{PMID Auto
|PMID=2703366
|Title=Hb G-Coushatta or alpha 2 beta 222(B4)Glu----Ala in a Turkish male.
}}

{{PMID Auto
|PMID=5658717
|Title=Hemoglobin variant common to Chinese and North American Indians: alpha-2-beta-22 Glu-Ala.
}}

{{PMID Auto
|PMID=5791015
|Title=Hemoglobin variant found in Koreans, Chinese, and North American Indians: alpha-2 beta-2 22 Glu Ala.
}}

{{PMID Auto
|PMID=9048934
|Title=Identification of novel Asian Indian and Japanese mutations causing beta-thalassaemia in the Egyptian population.
}}{{PMID Auto
|PMID=3623978
|Title=Hb G-Taipei or beta 22(B4)Glu----Gly in a Chinese family living in The Netherlands.
}}

{{PMID Auto
|PMID=6021187
|Title=Hemoglobin G Saskatoon: beta-22Glu--Ala.
}}

{{PMID Auto
|PMID=10081986
|Title=Genetic studies suggest a multicentric origin for Hb G-Coushatta [beta22(B4)Glu-->Ala].
}}

{{PMID Auto
|PMID=3446652
|Title=Hb D-Granada or alpha 2 beta 2 22(B4)Glu----Val.
}}