Canonical Allele Identifier: CA2580861029

Gene: IL33

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6256292G>C , CM000671.2:g.6256292G>C	GRCh38
NC_000009.11:g.6256292G>C , CM000671.1:g.6256292G>C	GRCh37
NC_000009.10:g.6246292G>C	NCBI36
NG_047209.1:g.46144G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_033439.4:c.*124G>C MANE Select	NP_254274.1:n.*124G>C
ENST00000682010.1:c.*124G>C MANE Select	ENSP00000507310.1:n.*124G>C
NM_001199640.1:c.*124G>C	NP_001186569.1:n.*124G>C
NM_001199640.2:c.*124G>C	NP_001186569.1:n.*124G>C
NM_001199641.1:c.*124G>C	NP_001186570.1:n.*124G>C
NM_001199641.2:c.*124G>C	NP_001186570.1:n.*124G>C
NM_001314044.1:c.*124G>C	NP_001300973.1:n.*124G>C
NM_001314044.2:c.*124G>C	NP_001300973.1:n.*124G>C
NM_001314045.1:c.*124G>C	NP_001300974.1:n.*124G>C
NM_001314045.2:c.*124G>C	NP_001300974.1:n.*124G>C
NM_001314046.1:c.*124G>C	NP_001300975.1:n.*124G>C
NM_001314046.2:c.*124G>C	NP_001300975.1:n.*124G>C
NM_001314047.1:c.*124G>C	NP_001300976.1:n.*124G>C
NM_001314047.2:c.*124G>C	NP_001300976.1:n.*124G>C
NM_001314048.1:c.*124G>C	NP_001300977.1:n.*124G>C
NM_001314048.2:c.*124G>C	NP_001300977.1:n.*124G>C
NM_001353802.1:c.*124G>C	NP_001340731.1:n.*124G>C
NM_001353802.2:c.*124G>C	NP_001340731.1:n.*124G>C
NM_033439.3:c.*124G>C	NP_254274.1:n.*124G>C
ENST00000381434.7:c.*124G>C	ENSP00000370842.3:n.*124G>C
ENST00000417746.6:c.*124G>C	ENSP00000394039.2:n.*124G>C
ENST00000456383.3:c.811G>C	ENSP00000414238.2:n.811G>C
XM_011518061.1:c.*124G>C	XP_011516363.1:n.*124G>C
XM_017015285.1:c.*124G>C	XP_016870774.1:n.*124G>C
XR_001746614.1:n.153-27997C>G