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April 10, 2026Transfusion0 citations

Identification of a novel nonsense variant ( c.184C>T ) in ABO*B.01 allele

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XBXiaoyun BuWZWei ZhangFSFeng Shao

Key Points

  • The study aims to identify and describe a novel nonsense variant within the ABO*B.01 allele.
  • Data collected from NCBI GenBank
  • Reference number provided for data access
  • Identification of variant c.184C>T
  • Novel allele variation reported
  • Data made publicly available for further analysis

Abstract

The authors have disclosed no conflicts of interest. The data that support the findings of this study are openly available in NCBI GenBank at https://www.ncbi.nlm.nih.gov/genbank/, reference number PX627881.

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Cite This Study

Bu et al. (2026) studied this question.

synapsesocial.com/papers/69d896166c1944d70ce074f1https://doi.org/10.1111/trf.70215
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