Canonical Allele Identifier: CA2660763932

Gene: IL1RN

Linked Data

• gnomAD v4: 2-113117945-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113117945T>A , CM000664.2:g.113117945T>A	GRCh38
NC_000002.11:g.113875522T>A , CM000664.1:g.113875522T>A	GRCh37
NC_000002.10:g.113591993T>A	NCBI36
NG_021240.1:g.5053T>A , LRG_188:g.5053T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2121T>A	ENSP00000387210.1:n.-272-2121T>A
ENST00000465812.6:n.775+280T>A
ENST00000696881.1:c.-356T>A	ENSP00000512949.1:n.-356T>A
ENST00000259206.9:c.-74T>A	ENSP00000259206.5:n.-74T>A
ENST00000354115.6:c.-74T>A	ENSP00000329072.3:n.-74T>A
ENST00000361779.7:c.-293T>A	ENSP00000354816.3:n.-293T>A
ENST00000409052.5:c.-272-2121T>A	ENSP00000387210.1:n.-272-2121T>A
NM_000577.4:c.-74T>A	NP_000568.1:n.-74T>A
NM_173841.2:c.-74T>A , LRG_188t1:c.-74T>A	NP_776213.1:n.-74T>A
NM_173843.2:c.-293T>A	NP_776215.1:n.-293T>A
XM_011511121.1:c.-272-2121T>A	XP_011509423.1:n.-272-2121T>A
NM_001318914.1:c.-356T>A	NP_001305843.1:n.-356T>A