Canonical Allele Identifier: CA13043016
Gene: IL33 HGNC NCBI

Linked Data

dbSNP Id: rs16924159
gnomAD v2: 9-6229417-G-A
gnomAD v3: 9-6229417-G-A
gnomAD v4: 9-6229417-G-A
MyVariant Identifiers: chr9:g.6229417G>A (hg19) chr9:g.6229417G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.6229417G>A , CM000671.2:g.6229417G>A GRCh38
NC_000009.11:g.6229417G>A , CM000671.1:g.6229417G>A GRCh37
NC_000009.10:g.6219417G>A NCBI36
NG_047209.1:g.19269G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682010.1:c.-11-12267G>A MANE Select ENSP00000507310.1:n.-11-12267G>A
ENST00000417746.6:c.-11-12267G>A ENSP00000394039.2:n.-11-12267G>A
NM_001199640.1:c.-11-12267G>A NP_001186569.1:n.-11-12267G>A
NM_001199641.1:c.-11-12267G>A NP_001186570.1:n.-11-12267G>A
NM_001314044.1:c.-11-12267G>A NP_001300973.1:n.-11-12267G>A
NM_001314046.1:c.-11-12267G>A NP_001300975.1:n.-11-12267G>A
NM_001314047.1:c.-11-12267G>A NP_001300976.1:n.-11-12267G>A
NM_001314048.1:c.-11-12267G>A NP_001300977.1:n.-11-12267G>A
NM_033439.3:c.-11-12267G>A NP_254274.1:n.-11-12267G>A
XM_017015285.1:c.-93-7644G>A XP_016870774.1:n.-93-7644G>A
XR_001746614.1:n.153-1122C>T
NM_001199640.2:c.-11-12267G>A NP_001186569.1:n.-11-12267G>A
NM_001314044.2:c.-11-12267G>A NP_001300973.1:n.-11-12267G>A
NM_001314046.2:c.-11-12267G>A NP_001300975.1:n.-11-12267G>A
NM_001314047.2:c.-11-12267G>A NP_001300976.1:n.-11-12267G>A
NM_001314048.2:c.-11-12267G>A NP_001300977.1:n.-11-12267G>A
NM_033439.4:c.-11-12267G>A MANE Select NP_254274.1:n.-11-12267G>A
NM_001199641.2:c.-11-12267G>A NP_001186570.1:n.-11-12267G>A
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