Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.148827884G>ACA447425597ADRB2c.1053G>A (p.Gly351=)
dbSNP gnomAD v4
5g.148827884G>CCA3498500ADRB2c.1053G>C (p.Gly351=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.148827884G=CA1590223899ADRB2c.1053G= (p.Gly351=)
dbSNP

Number of alleles fetched