Canonical Allele Identifier: CA188630783

Gene: IL33

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6241737G>A , CM000671.2:g.6241737G>A	GRCh38
NC_000009.11:g.6241737G>A , CM000671.1:g.6241737G>A	GRCh37
NC_000009.10:g.6231737G>A	NCBI36
NG_047209.1:g.31589G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_033439.4:c.43G>A MANE Select	NP_254274.1:p.Ala15Thr
ENST00000682010.1:c.43G>A MANE Select	ENSP00000507310.1:p.Ala15Thr
NM_001199640.1:c.43G>A	NP_001186569.1:p.Ala15Thr
NM_001199640.2:c.43G>A	NP_001186569.1:p.Ala15Thr
NM_001199641.1:c.43G>A	NP_001186570.1:p.Ala15Thr
NM_001199641.2:c.43G>A	NP_001186570.1:p.Ala15Thr
NM_001314044.1:c.43G>A	NP_001300973.1:p.Ala15Thr
NM_001314044.2:c.43G>A	NP_001300973.1:p.Ala15Thr
NM_001314045.1:c.43G>A	NP_001300974.1:p.Ala15Thr
NM_001314045.2:c.43G>A	NP_001300974.1:p.Ala15Thr
NM_001314046.1:c.43G>A	NP_001300975.1:p.Ala15Thr
NM_001314046.2:c.43G>A	NP_001300975.1:p.Ala15Thr
NM_001314047.1:c.43G>A	NP_001300976.1:p.Ala15Thr
NM_001314047.2:c.43G>A	NP_001300976.1:p.Ala15Thr
NM_001314048.1:c.43G>A	NP_001300977.1:p.Ala15Thr
NM_001314048.2:c.43G>A	NP_001300977.1:p.Ala15Thr
NM_033439.3:c.43G>A	NP_254274.1:p.Ala15Thr
ENST00000381434.7:c.43G>A	ENSP00000370842.3:p.Ala15Thr
ENST00000417746.6:c.43G>A	ENSP00000394039.2:p.Ala15Thr
ENST00000456383.3:c.43G>A	ENSP00000414238.2:p.Ala15Thr
ENST00000463336.1:n.45G>A
ENST00000611532.4:c.43G>A	ENSP00000478858.1:p.Ala15Thr
XM_017015285.1:c.43G>A	XP_016870774.1:p.Ala15Thr
XR_001746614.1:n.153-13442C>T