Canonical Allele Identifier: CA4978929

Gene: IL33

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6254512G>C , CM000671.2:g.6254512G>C	GRCh38
NC_000009.11:g.6254512G>C , CM000671.1:g.6254512G>C	GRCh37
NC_000009.10:g.6244512G>C	NCBI36
NG_047209.1:g.44364G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682010.1:c.571G>C MANE Select	ENSP00000507310.1:p.Asp191His
ENST00000381434.7:c.571G>C	ENSP00000370842.3:p.Asp191His
ENST00000417746.6:c.193G>C	ENSP00000394039.2:p.Asp65His
ENST00000456383.3:c.445G>C	ENSP00000414238.2:p.Asp149His
ENST00000611532.4:c.445G>C	ENSP00000478858.1:p.Asp149His
NM_001199640.1:c.445G>C	NP_001186569.1:p.Asp149His
NM_001199641.1:c.193G>C	NP_001186570.1:p.Asp65His
NM_001314044.1:c.571G>C	NP_001300973.1:p.Asp191His
NM_001314045.1:c.571G>C	NP_001300974.1:p.Asp191His
NM_001314046.1:c.553G>C	NP_001300975.1:p.Asp185His
NM_001314047.1:c.553G>C	NP_001300976.1:p.Asp185His
NM_001314048.1:c.445G>C	NP_001300977.1:p.Asp149His
NM_033439.3:c.571G>C	NP_254274.1:p.Asp191His
XM_011518061.1:c.448G>C	XP_011516363.1:p.Asp150His
NM_001353802.1:c.448G>C	NP_001340731.1:p.Asp150His
XM_017015285.1:c.553G>C	XP_016870774.1:p.Asp185His
XR_001746614.1:n.153-26217C>G
NM_001199640.2:c.445G>C	NP_001186569.1:p.Asp149His
NM_001314044.2:c.571G>C	NP_001300973.1:p.Asp191His
NM_001314045.2:c.571G>C	NP_001300974.1:p.Asp191His
NM_001314046.2:c.553G>C	NP_001300975.1:p.Asp185His
NM_001314047.2:c.553G>C	NP_001300976.1:p.Asp185His
NM_001314048.2:c.445G>C	NP_001300977.1:p.Asp149His
NM_001353802.2:c.448G>C	NP_001340731.1:p.Asp150His
NM_033439.4:c.571G>C MANE Select	NP_254274.1:p.Asp191His
NM_001199641.2:c.193G>C	NP_001186570.1:p.Asp65His