Canonical Allele Identifier: CA2660763978

Gene: IL1RN

Linked Data

• gnomAD v4: 2-113118004-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113118004T>A , CM000664.2:g.113118004T>A	GRCh38
NC_000002.11:g.113875581T>A , CM000664.1:g.113875581T>A	GRCh37
NC_000002.10:g.113592052T>A	NCBI36
NG_021240.1:g.5112T>A , LRG_188:g.5112T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2062T>A	ENSP00000387210.1:n.-272-2062T>A
ENST00000465812.6:n.775+339T>A
ENST00000696881.1:c.-297T>A	ENSP00000512949.1:n.-297T>A
ENST00000259206.9:c.-15T>A	ENSP00000259206.5:n.-15T>A
ENST00000354115.6:c.-15T>A	ENSP00000329072.3:n.-15T>A
ENST00000361779.7:c.-234T>A	ENSP00000354816.3:n.-234T>A
ENST00000409052.5:c.-272-2062T>A	ENSP00000387210.1:n.-272-2062T>A
ENST00000486167.1:n.24T>A
NM_000577.4:c.-15T>A	NP_000568.1:n.-15T>A
NM_173841.2:c.-15T>A , LRG_188t1:c.-15T>A	NP_776213.1:n.-15T>A
NM_173843.2:c.-234T>A	NP_776215.1:n.-234T>A
XM_006712497.2:c.-297T>A	XP_006712560.1:n.-297T>A
XM_011511121.1:c.-272-2062T>A	XP_011509423.1:n.-272-2062T>A
NM_001318914.1:c.-297T>A	NP_001305843.1:n.-297T>A
NM_000577.5:c.-15T>A	NP_000568.1:n.-15T>A
NM_001318914.2:c.-297T>A	NP_001305843.1:n.-297T>A
NM_173843.3:c.-234T>A	NP_776215.1:n.-234T>A
NM_173841.3:c.-15T>A	NP_776213.1:n.-15T>A