Canonical Allele Identifier: CA2689334432
Gene: IL33 HGNC NCBI

Linked Data

gnomAD v4: 9-6253481-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6253481A>T , CM000671.2:g.6253481A>T GRCh38
NC_000009.11:g.6253481A>T , CM000671.1:g.6253481A>T GRCh37
NC_000009.10:g.6243481A>T NCBI36
NG_047209.1:g.43333A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682010.1:c.470-71A>T MANE Select ENSP00000507310.1:n.470-71A>T
ENST00000381434.7:c.470-71A>T ENSP00000370842.3:n.470-71A>T
ENST00000417746.6:c.92-71A>T ENSP00000394039.2:n.92-71A>T
ENST00000456383.3:c.344-71A>T ENSP00000414238.2:n.344-71A>T
ENST00000611532.4:c.344-71A>T ENSP00000478858.1:n.344-71A>T
NM_001199640.1:c.344-71A>T NP_001186569.1:n.344-71A>T
NM_001199641.1:c.92-71A>T NP_001186570.1:n.92-71A>T
NM_001314044.1:c.470-71A>T NP_001300973.1:n.470-71A>T
NM_001314045.1:c.470-71A>T NP_001300974.1:n.470-71A>T
NM_001314046.1:c.452-71A>T NP_001300975.1:n.452-71A>T
NM_001314047.1:c.452-71A>T NP_001300976.1:n.452-71A>T
NM_001314048.1:c.344-71A>T NP_001300977.1:n.344-71A>T
NM_033439.3:c.470-71A>T NP_254274.1:n.470-71A>T
XM_011518061.1:c.347-71A>T XP_011516363.1:n.347-71A>T
NM_001353802.1:c.347-71A>T NP_001340731.1:n.347-71A>T
XM_017015285.1:c.452-71A>T XP_016870774.1:n.452-71A>T
XR_001746614.1:n.153-25186T>A
NM_001199640.2:c.344-71A>T NP_001186569.1:n.344-71A>T
NM_001314044.2:c.470-71A>T NP_001300973.1:n.470-71A>T
NM_001314045.2:c.470-71A>T NP_001300974.1:n.470-71A>T
NM_001314046.2:c.452-71A>T NP_001300975.1:n.452-71A>T
NM_001314047.2:c.452-71A>T NP_001300976.1:n.452-71A>T
NM_001314048.2:c.344-71A>T NP_001300977.1:n.344-71A>T
NM_001353802.2:c.347-71A>T NP_001340731.1:n.347-71A>T
NM_033439.4:c.470-71A>T MANE Select NP_254274.1:n.470-71A>T
NM_001199641.2:c.92-71A>T NP_001186570.1:n.92-71A>T