Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.151688291C>ACA16603998NEBc.2415+1G>T (n.2415+1G>T)
ClinVar dbSNP
2g.151688291C>TCA16617246NEBc.2415+1G>A (n.2415+1G>A)
ClinVar dbSNP gnomAD v4

Number of alleles fetched