Canonical Allele Identifier: CA2577114139

Gene: IL1RN

Linked Data

• gnomAD v4: 2-113117966-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113117966G>C , CM000664.2:g.113117966G>C	GRCh38
NC_000002.11:g.113875543G>C , CM000664.1:g.113875543G>C	GRCh37
NC_000002.10:g.113592014G>C	NCBI36
NG_021240.1:g.5074G>C , LRG_188:g.5074G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2100G>C	ENSP00000387210.1:n.-272-2100G>C
ENST00000465812.6:n.775+301G>C
ENST00000696881.1:c.-335G>C	ENSP00000512949.1:n.-335G>C
ENST00000259206.9:c.-53G>C	ENSP00000259206.5:n.-53G>C
ENST00000354115.6:c.-53G>C	ENSP00000329072.3:n.-53G>C
ENST00000361779.7:c.-272G>C	ENSP00000354816.3:n.-272G>C
ENST00000409052.5:c.-272-2100G>C	ENSP00000387210.1:n.-272-2100G>C
NM_000577.4:c.-53G>C	NP_000568.1:n.-53G>C
NM_173841.2:c.-53G>C , LRG_188t1:c.-53G>C	NP_776213.1:n.-53G>C
NM_173843.2:c.-272G>C	NP_776215.1:n.-272G>C
XM_011511121.1:c.-272-2100G>C	XP_011509423.1:n.-272-2100G>C
NM_001318914.1:c.-335G>C	NP_001305843.1:n.-335G>C