Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47349923C>ACA015338MYBPC3c.506-1G>T (n.506-1G>T)
ClinVar dbSNP gnomAD v4
11g.47349923C>TCA380338276MYBPC3c.506-1G>A (n.506-1G>A)
ClinVar dbSNP
11g.47349923C>GCA015332MYBPC3c.506-1G>C (n.506-1G>C)
dbSNP
11g.47349923C=CA1969341805MYBPC3c.506-1G= (n.506-1G=)
dbSNP

Number of alleles fetched