Canonical Allele Identifier: CA1838879

Gene: IL1RN

Linked Data

• ClinVar Variation Id: 1520575
• ClinVar RCV Id: RCV002030838
• dbSNP Id: rs767854418
• ExAC: 2:113890257 G / A
• gnomAD v2: 2-113890257-G-A
• gnomAD v3: 2-113132680-G-A
• gnomAD v4: 2-113132680-G-A
• MyVariant Identifiers: chr2:g.113890257G>A (hg19) ; chr2:g.113132680G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132680G>A , CM000664.2:g.113132680G>A	GRCh38
NC_000002.11:g.113890257G>A , CM000664.1:g.113890257G>A	GRCh37
NC_000002.10:g.113606728G>A	NCBI36
NG_021240.1:g.19788G>A , LRG_188:g.19788G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.241G>A	ENSP00000387210.1:p.Glu81Lys
ENST00000696879.1:c.241G>A	ENSP00000512947.1:p.Glu81Lys
ENST00000696880.1:c.241G>A	ENSP00000512948.1:p.Glu81Lys
ENST00000696881.1:c.241G>A	ENSP00000512949.1:p.Glu81Lys
ENST00000696882.1:c.*113G>A	ENSP00000512950.1:n.*113G>A
ENST00000696883.1:n.288G>A
ENST00000409930.4:c.343G>A MANE Select	ENSP00000387173.3:p.Glu115Lys
ENST00000259206.9:c.352G>A	ENSP00000259206.5:p.Glu118Lys
ENST00000354115.6:c.289G>A	ENSP00000329072.3:p.Glu97Lys
ENST00000361779.7:c.241G>A	ENSP00000354816.3:p.Glu81Lys
ENST00000409052.5:c.241G>A	ENSP00000387210.1:p.Glu81Lys
ENST00000409930.3:c.343G>A	ENSP00000387173.3:p.Glu115Lys
NM_000577.4:c.289G>A	NP_000568.1:p.Glu97Lys
NM_173841.2:c.352G>A , LRG_188t1:c.352G>A	NP_776213.1:p.Glu118Lys
NM_173842.2:c.343G>A	NP_776214.1:p.Glu115Lys
NM_173843.2:c.241G>A	NP_776215.1:p.Glu81Lys
XM_005263661.3:c.241G>A	XP_005263718.1:p.Glu81Lys
XM_006712497.2:c.241G>A	XP_006712560.1:p.Glu81Lys
XM_011511121.1:c.241G>A	XP_011509423.1:p.Glu81Lys
NM_001318914.1:c.241G>A	NP_001305843.1:p.Glu81Lys
XM_005263661.4:c.241G>A	XP_005263718.1:p.Glu81Lys
NM_000577.5:c.289G>A	NP_000568.1:p.Glu97Lys
NM_001318914.2:c.241G>A	NP_001305843.1:p.Glu81Lys
NM_173842.3:c.343G>A MANE Select	NP_776214.1:p.Glu115Lys
NM_173843.3:c.241G>A	NP_776215.1:p.Glu81Lys
NM_001379360.1:c.241G>A	NP_001366289.1:p.Glu81Lys
NM_173841.3:c.352G>A	NP_776213.1:p.Glu118Lys