Hemoglobin G Georgia is a rare variant of the hemoglobin molecule, specifically a hemoglobinopathy, caused by a mutation in the HBG2 gene. This genetic condition results in the production of an abnormal form of hemoglobin, which can lead to mild to moderate anemia. The mutation replaces a single amino acid in the hemoglobin molecule, affecting its structure and function. Hemoglobin G Georgia is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to express the condition. While it is more prevalent in certain populations, such as those of African descent, it can occur in any individual with the necessary genetic background. The symptoms and severity of the condition can vary, and treatment may include management of anemia and monitoring for potential complications.
The CAS Registry Mumber 9034-71-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 9,0,3 and 4 respectively; the second part has 2 digits, 7 and 1 respectively. Calculate Digit Verification of CAS Registry Number 9034-71: (6*9)+(5*0)+(4*3)+(3*4)+(2*7)+(1*1)=93 93 % 10 = 3 So 9034-71-3 is a valid CAS Registry Number.