Canonical Allele Identifier: CA348294693

Gene: IL1RN

Linked Data

• ClinVar Variation Id: 660469
• ClinVar RCV Id: RCV000817668
• dbSNP Id: rs1203011392
• gnomAD v4: 2-113129644-G-A
• COSMIC: COSM3565489 ; COSM3565490
• MyVariant Identifiers: chr2:g.113887221G>A (hg19) ; chr2:g.113129644G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113129644G>A , CM000664.2:g.113129644G>A	GRCh38
NC_000002.11:g.113887221G>A , CM000664.1:g.113887221G>A	GRCh37
NC_000002.10:g.113603692G>A	NCBI36
NG_021240.1:g.16752G>A , LRG_188:g.16752G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.83G>A	ENSP00000387210.1:p.Gly28Glu
ENST00000696879.1:c.83G>A	ENSP00000512947.1:p.Gly28Glu
ENST00000696880.1:c.83G>A	ENSP00000512948.1:p.Gly28Glu
ENST00000696881.1:c.83G>A	ENSP00000512949.1:p.Gly28Glu
ENST00000696882.1:c.83G>A	ENSP00000512950.1:p.Gly28Glu
ENST00000409930.4:c.185G>A MANE Select	ENSP00000387173.3:p.Gly62Glu
ENST00000259206.9:c.194G>A	ENSP00000259206.5:p.Gly65Glu
ENST00000354115.6:c.131G>A	ENSP00000329072.3:p.Gly44Glu
ENST00000361779.7:c.83G>A	ENSP00000354816.3:p.Gly28Glu
ENST00000409052.5:c.83G>A	ENSP00000387210.1:p.Gly28Glu
ENST00000409930.3:c.185G>A	ENSP00000387173.3:p.Gly62Glu
ENST00000472292.1:n.234G>A
ENST00000486167.1:n.169G>A
NM_000577.4:c.131G>A	NP_000568.1:p.Gly44Glu
NM_173841.2:c.194G>A , LRG_188t1:c.194G>A	NP_776213.1:p.Gly65Glu
NM_173842.2:c.185G>A	NP_776214.1:p.Gly62Glu
NM_173843.2:c.83G>A	NP_776215.1:p.Gly28Glu
XM_005263661.3:c.83G>A	XP_005263718.1:p.Gly28Glu
XM_006712497.2:c.83G>A	XP_006712560.1:p.Gly28Glu
XM_011511121.1:c.83G>A	XP_011509423.1:p.Gly28Glu
NM_001318914.1:c.83G>A	NP_001305843.1:p.Gly28Glu
XM_005263661.4:c.83G>A	XP_005263718.1:p.Gly28Glu
NM_000577.5:c.131G>A	NP_000568.1:p.Gly44Glu
NM_001318914.2:c.83G>A	NP_001305843.1:p.Gly28Glu
NM_173842.3:c.185G>A MANE Select	NP_776214.1:p.Gly62Glu
NM_173843.3:c.83G>A	NP_776215.1:p.Gly28Glu
NM_001379360.1:c.83G>A	NP_001366289.1:p.Gly28Glu
NM_173841.3:c.194G>A	NP_776213.1:p.Gly65Glu