Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.154587511C>ACA126508FGAc.510+1G>T (n.510+1G>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.154587511C>GCA3115285FGAc.510+1G>C (n.510+1G>C)
ClinVar dbSNP ExAC gnomAD v2
4g.154587511C=CA1504944027FGAc.510+1G= (n.510+1G=)
dbSNP

Number of alleles fetched