Canonical Allele Identifier: CA1830320731
Community Standard Title: NM_033439.4(IL33):c.92-3044C=
Gene: IL33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6247430C= , CM000671.2:g.6247430C= GRCh38
NC_000009.11:g.6247430C= , CM000671.1:g.6247430C= GRCh37
NC_000009.10:g.6237430C= NCBI36
NG_047209.1:g.37282C=

Transcript Alleles

HGVS Amino-acid Change
NM_033439.4:c.92-3044C= MANE Select NP_254274.1:n.92-3044C=
ENST00000682010.1:c.92-3044C= MANE Select ENSP00000507310.1:n.92-3044C=
NM_001199640.1:c.92-3044C= NP_001186569.1:n.92-3044C=
NM_001199640.2:c.92-3044C= NP_001186569.1:n.92-3044C=
NM_001199641.1:c.91+5645C= NP_001186570.1:n.91+5645C=
NM_001199641.2:c.91+5645C= NP_001186570.1:n.91+5645C=
NM_001314044.1:c.92-3044C= NP_001300973.1:n.92-3044C=
NM_001314044.2:c.92-3044C= NP_001300973.1:n.92-3044C=
NM_001314045.1:c.92-3044C= NP_001300974.1:n.92-3044C=
NM_001314045.2:c.92-3044C= NP_001300974.1:n.92-3044C=
NM_001314046.1:c.92-3044C= NP_001300975.1:n.92-3044C=
NM_001314046.2:c.92-3044C= NP_001300975.1:n.92-3044C=
NM_001314047.1:c.92-3044C= NP_001300976.1:n.92-3044C=
NM_001314047.2:c.92-3044C= NP_001300976.1:n.92-3044C=
NM_001314048.1:c.92-3044C= NP_001300977.1:n.92-3044C=
NM_001314048.2:c.92-3044C= NP_001300977.1:n.92-3044C=
NM_033439.3:c.92-3044C= NP_254274.1:n.92-3044C=
ENST00000381434.7:c.92-3044C= ENSP00000370842.3:n.92-3044C=
ENST00000417746.6:c.91+5645C= ENSP00000394039.2:n.91+5645C=
ENST00000456383.3:c.92-3044C= ENSP00000414238.2:n.92-3044C=
ENST00000611532.4:c.92-3044C= ENSP00000478858.1:n.92-3044C=
XM_017015285.1:c.92-3044C= XP_016870774.1:n.92-3044C=
XR_001746614.1:n.153-19135G=