Canonical Allele Identifier: CA2651722304
Gene: ADAM33 HGNC NCBI

Linked Data

gnomAD v4: 20-3667971-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3667971A>G , CM000682.2:g.3667971A>G GRCh38
NC_000020.10:g.3648618A>G , CM000682.1:g.3648618A>G GRCh37
NC_000020.9:g.3596618A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.6:c.*992T>C ENSP00000348912.2:n.*992T>C
ENST00000379861.8:c.*992T>C ENSP00000369190.4:n.*992T>C
ENST00000466620.5:n.2995T>C
ENST00000483362.1:n.2357T>C
NM_001282447.2:c.*992T>C NP_001269376.1:n.*992T>C
NM_025220.4:c.*992T>C NP_079496.1:n.*992T>C
NM_153202.3:c.*992T>C NP_694882.1:n.*992T>C