Canonical Allele Identifier: CA16354115

Gene: IL33

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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