Canonical Allele Identifier: CA53698028

Gene: IL1RN

Linked Data

• ClinVar Variation Id: 3000427
• ClinVar RCV Id: RCV003857602
• dbSNP Id: rs4252024
• gnomAD v3: 2-113132871-G-A
• gnomAD v4: 2-113132871-G-A
• MyVariant Identifiers: chr2:g.113890448G>A (hg19) ; chr2:g.113132871G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132871G>A , CM000664.2:g.113132871G>A	GRCh38
NC_000002.11:g.113890448G>A , CM000664.1:g.113890448G>A	GRCh37
NC_000002.10:g.113606919G>A	NCBI36
NG_021240.1:g.19979G>A , LRG_188:g.19979G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.432G>A	ENSP00000387210.1:p.Ter144=
ENST00000696879.1:c.432G>A	ENSP00000512947.1:p.Ter144=
ENST00000696880.1:c.432G>A	ENSP00000512948.1:p.Ter144=
ENST00000696881.1:c.432G>A	ENSP00000512949.1:p.Ter144=
ENST00000696882.1:c.*304G>A	ENSP00000512950.1:n.*304G>A
ENST00000696883.1:n.479G>A
ENST00000409930.4:c.534G>A MANE Select	ENSP00000387173.3:p.Ter178=
ENST00000259206.9:c.543G>A	ENSP00000259206.5:p.Ter181=
ENST00000354115.6:c.480G>A	ENSP00000329072.3:p.Ter160=
ENST00000361779.7:c.432G>A	ENSP00000354816.3:p.Ter144=
ENST00000409052.5:c.432G>A	ENSP00000387210.1:p.Ter144=
ENST00000409930.3:c.534G>A	ENSP00000387173.3:p.Ter178=
NM_000577.4:c.480G>A	NP_000568.1:p.Ter160=
NM_173841.2:c.543G>A , LRG_188t1:c.543G>A	NP_776213.1:p.Ter181=
NM_173842.2:c.534G>A	NP_776214.1:p.Ter178=
NM_173843.2:c.432G>A	NP_776215.1:p.Ter144=
XM_005263661.3:c.432G>A	XP_005263718.1:p.Ter144=
XM_006712497.2:c.432G>A	XP_006712560.1:p.Ter144=
XM_011511121.1:c.432G>A	XP_011509423.1:p.Ter144=
NM_001318914.1:c.432G>A	NP_001305843.1:p.Ter144=
XM_005263661.4:c.432G>A	XP_005263718.1:p.Ter144=
NM_000577.5:c.480G>A	NP_000568.1:p.Ter160=
NM_001318914.2:c.432G>A	NP_001305843.1:p.Ter144=
NM_173842.3:c.534G>A MANE Select	NP_776214.1:p.Ter178=
NM_173843.3:c.432G>A	NP_776215.1:p.Ter144=
NM_001379360.1:c.432G>A	NP_001366289.1:p.Ter144=
NM_173841.3:c.543G>A	NP_776213.1:p.Ter181=