Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.29220734G>TCA16602591ALKc.3617C>A (p.Ser1206Tyr)
c.844C>A
n.494C>A
c.413C>A (p.Ser138Tyr)
c.497C>A (p.Ser166Tyr)
c.2486C>A (p.Ser829Tyr)
c.770C>A (p.Ser257Tyr)
ClinVar dbSNP COSMIC
2g.29220734G>CCA346472998ALKc.3617C>G (p.Ser1206Cys)
c.844C>G
n.494C>G
c.413C>G (p.Ser138Cys)
c.497C>G (p.Ser166Cys)
c.2486C>G (p.Ser829Cys)
c.770C>G (p.Ser257Cys)
dbSNP
2g.29220734G>ACA346472997ALKc.3617C>T (p.Ser1206Phe)
c.844C>T
n.494C>T
c.413C>T (p.Ser138Phe)
c.497C>T (p.Ser166Phe)
c.2486C>T (p.Ser829Phe)
c.770C>T (p.Ser257Phe)
dbSNP

Number of alleles fetched