Canonical Allele Identifier: CA53685528

Gene: IL1RN

Linked Data

• dbSNP Id: rs939552946
• gnomAD v3: 2-113117914-G-T
• gnomAD v4: 2-113117914-G-T
• MyVariant Identifiers: chr2:g.113875491G>T (hg19) ; chr2:g.113117914G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113117914G>T , CM000664.2:g.113117914G>T	GRCh38
NC_000002.11:g.113875491G>T , CM000664.1:g.113875491G>T	GRCh37
NC_000002.10:g.113591962G>T	NCBI36
NG_021240.1:g.5022G>T , LRG_188:g.5022G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2152G>T	ENSP00000387210.1:n.-272-2152G>T
ENST00000465812.6:n.775+249G>T
ENST00000259206.9:c.-105G>T	ENSP00000259206.5:n.-105G>T
ENST00000354115.6:c.-105G>T	ENSP00000329072.3:n.-105G>T
ENST00000361779.7:c.-324G>T	ENSP00000354816.3:n.-324G>T
ENST00000409052.5:c.-272-2152G>T	ENSP00000387210.1:n.-272-2152G>T
NM_000577.4:c.-105G>T	NP_000568.1:n.-105G>T
NM_173841.2:c.-105G>T , LRG_188t1:c.-105G>T	NP_776213.1:n.-105G>T
NM_173843.2:c.-324G>T	NP_776215.1:n.-324G>T
XM_011511121.1:c.-272-2152G>T	XP_011509423.1:n.-272-2152G>T
NM_001318914.1:c.-387G>T	NP_001305843.1:n.-387G>T