Canonical Allele Identifier: CA2346676889
Gene: ADAM33 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3667970T= , CM000682.2:g.3667970T= GRCh38
NC_000020.10:g.3648617T= , CM000682.1:g.3648617T= GRCh37
NC_000020.9:g.3596617T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.6:c.*993A= ENSP00000348912.2:n.*993A=
ENST00000379861.8:c.*993A= ENSP00000369190.4:n.*993A=
ENST00000466620.5:n.2996A=
ENST00000483362.1:n.2358A=
NM_001282447.2:c.*993A= NP_001269376.1:n.*993A=
NM_025220.4:c.*993A= NP_079496.1:n.*993A=
NM_153202.3:c.*993A= NP_694882.1:n.*993A=
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