Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.67436797T>CCA129702HSD11B2c.1012T>C (p.Tyr338His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.67436797T>GCA396283896HSD11B2c.1012T>G (p.Tyr338Asp)
dbSNP gnomAD v4
16g.67436797T=CA2229310666HSD11B2c.1012T= (p.Tyr338=)
dbSNP

Number of alleles fetched