{{Rsnum
|rsid=111033605
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA2
|position=173003
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=111033605
|variant=0054
}}{{ClinVar
|ALT=A,C
|CHROM=16
|CLNALLE=2
|CLNHGVS=NC_000016.9:g.223002G>C
|CLNORIGIN=1
|CLNSIG=255
|FwdALT=A,C
|FwdREF=G
|GENEINFO=HBA2:3040
|GENE_ID=3040
|GENE_NAME=HBA2
|REF=G
|RSPOS=223002
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=132
|rsid=111033605
|CLNACC=RCV000016963.1; RCV000016964.1; RCV000016965.1; RCV000016966.1
|CLNDBN=HEMOGLOBIN G (HONOLULU); HEMOGLOBIN G (HONG KONG); HEMOGLOBIN G (SINGAPORE); HEMOGLOBIN G (CHINESE)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141800.0039; 141850.0054
|Disease=HEMOGLOBIN G (HONOLULU); HEMOGLOBIN G (HONG KONG); HEMOGLOBIN G (SINGAPORE); HEMOGLOBIN G (CHINESE)
}}{{PMID Auto
|PMID=2117321
|Title=Hb O Padova in a Spanish Family.
}}

{{PMID Auto
|PMID=2869010
|Title=Hemoglobin O-Padova or alpha(2)30(B11)Glu----Lys beta 2 observed in members of a Turkish family.
}}

{{PMID Auto
|PMID=4429803
|Title=A new abnormal hemoglobin O Padova, alpha 30 (B11) Glu -- Lys, and a dyserythropoietic anemia with erythroblastic multinuclearity coexisting in the same patient.
}}

{{PMID Auto
|PMID=6866546
|Title=Association between Hb O Padova [alpha 30 (B 11) Glu leads to Lys] and Rendu-Osler disease.
}}

{{PMID Auto
|PMID=9215129
|Title=Haemoglobin O Padova and falsely low haemoglobin A1c in a patient with type I diabetes.
|OA=1
}}

{{PMID Auto
|PMID=10868862
|Title=Evaluation of HbA1c determination methods in patients with hemoglobinopathies.
}}

{{PMID Auto
|PMID=12195002
|Title=Silent haemoglobin variants and determination of HbA(1c) with the HPLC Bio-Rad Variant II.
|OA=1
}}

{{PMID Auto
|PMID=5081025
|Title=Hemoglobin G Chinese in Chinese subjects in Taiwan.
}}

{{PMID Auto
|PMID=6238696
|Title=[A case of HbG Chinese found in Henan].
}}

{{PMID Auto
|PMID=11939521
|Title=Hb G-Chinese: a G-->C substitution at codon 30 of the alpha2-globin gene creates a PstI cutting site.
}}

{{PMID Auto
|PMID=12403500
|Title=Hb G-Honolulu [alpha30(B11)Glu-->Gln (alpha2)], Hb J-Meinung [beta56(D7)Gly-->Asp], and beta-thalassemia [codons 41/42 (-TCTT)] in a Taiwanese family.
}}