Canonical Allele Identifier: CA1830316975
Gene: IL33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6231239A= , CM000671.2:g.6231239A= GRCh38
NC_000009.11:g.6231239A= , CM000671.1:g.6231239A= GRCh37
NC_000009.10:g.6221239A= NCBI36
NG_047209.1:g.21091A=

Transcript Alleles

HGVS Amino-acid Change
NM_033439.4:c.-11-10445A= MANE Select NP_254274.1:n.-11-10445A=
ENST00000682010.1:c.-11-10445A= MANE Select ENSP00000507310.1:n.-11-10445A=
NM_001199640.1:c.-11-10445A= NP_001186569.1:n.-11-10445A=
NM_001199640.2:c.-11-10445A= NP_001186569.1:n.-11-10445A=
NM_001199641.1:c.-11-10445A= NP_001186570.1:n.-11-10445A=
NM_001199641.2:c.-11-10445A= NP_001186570.1:n.-11-10445A=
NM_001314044.1:c.-11-10445A= NP_001300973.1:n.-11-10445A=
NM_001314044.2:c.-11-10445A= NP_001300973.1:n.-11-10445A=
NM_001314046.1:c.-11-10445A= NP_001300975.1:n.-11-10445A=
NM_001314046.2:c.-11-10445A= NP_001300975.1:n.-11-10445A=
NM_001314047.1:c.-11-10445A= NP_001300976.1:n.-11-10445A=
NM_001314047.2:c.-11-10445A= NP_001300976.1:n.-11-10445A=
NM_001314048.1:c.-11-10445A= NP_001300977.1:n.-11-10445A=
NM_001314048.2:c.-11-10445A= NP_001300977.1:n.-11-10445A=
NM_033439.3:c.-11-10445A= NP_254274.1:n.-11-10445A=
ENST00000417746.6:c.-11-10445A= ENSP00000394039.2:n.-11-10445A=
XM_017015285.1:c.-93-5822A= XP_016870774.1:n.-93-5822A=
XR_001746614.1:n.153-2944T=