Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.5234175T>CCA124695HBDc.131A>G (p.Glu44Gly)
c.92+167A>G (n.92+167A>G)
ClinVar dbSNP gnomAD v4
11g.5234175T=CA1949565337HBDc.131A= (p.Glu44=)
c.92+167A= (n.92+167A=)
dbSNP

Number of alleles fetched