Canonical Allele Identifier: CA348296086

Gene: IL1RN

Linked Data

• dbSNP Id: rs1687217114
• gnomAD v3: 2-113132728-G-A
• gnomAD v4: 2-113132728-G-A
• COSMIC: COSM4546519 ; COSM4546520 ; COSM4546521
• MyVariant Identifiers: chr2:g.113890305G>A (hg19) ; chr2:g.113132728G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132728G>A , CM000664.2:g.113132728G>A	GRCh38
NC_000002.11:g.113890305G>A , CM000664.1:g.113890305G>A	GRCh37
NC_000002.10:g.113606776G>A	NCBI36
NG_021240.1:g.19836G>A , LRG_188:g.19836G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.289G>A	ENSP00000387210.1:p.Gly97Ser
ENST00000696879.1:c.289G>A	ENSP00000512947.1:p.Gly97Ser
ENST00000696880.1:c.289G>A	ENSP00000512948.1:p.Gly97Ser
ENST00000696881.1:c.289G>A	ENSP00000512949.1:p.Gly97Ser
ENST00000696882.1:c.*161G>A	ENSP00000512950.1:n.*161G>A
ENST00000696883.1:n.336G>A
ENST00000409930.4:c.391G>A MANE Select	ENSP00000387173.3:p.Gly131Ser
ENST00000259206.9:c.400G>A	ENSP00000259206.5:p.Gly134Ser
ENST00000354115.6:c.337G>A	ENSP00000329072.3:p.Gly113Ser
ENST00000361779.7:c.289G>A	ENSP00000354816.3:p.Gly97Ser
ENST00000409052.5:c.289G>A	ENSP00000387210.1:p.Gly97Ser
ENST00000409930.3:c.391G>A	ENSP00000387173.3:p.Gly131Ser
NM_000577.4:c.337G>A	NP_000568.1:p.Gly113Ser
NM_173841.2:c.400G>A , LRG_188t1:c.400G>A	NP_776213.1:p.Gly134Ser
NM_173842.2:c.391G>A	NP_776214.1:p.Gly131Ser
NM_173843.2:c.289G>A	NP_776215.1:p.Gly97Ser
XM_005263661.3:c.289G>A	XP_005263718.1:p.Gly97Ser
XM_006712497.2:c.289G>A	XP_006712560.1:p.Gly97Ser
XM_011511121.1:c.289G>A	XP_011509423.1:p.Gly97Ser
NM_001318914.1:c.289G>A	NP_001305843.1:p.Gly97Ser
XM_005263661.4:c.289G>A	XP_005263718.1:p.Gly97Ser
NM_000577.5:c.337G>A	NP_000568.1:p.Gly113Ser
NM_001318914.2:c.289G>A	NP_001305843.1:p.Gly97Ser
NM_173842.3:c.391G>A MANE Select	NP_776214.1:p.Gly131Ser
NM_173843.3:c.289G>A	NP_776215.1:p.Gly97Ser
NM_001379360.1:c.289G>A	NP_001366289.1:p.Gly97Ser
NM_173841.3:c.400G>A	NP_776213.1:p.Gly134Ser