Canonical Allele Identifier: CA1280066372
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs1686632488

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113117901C>T , CM000664.2:g.113117901C>T GRCh38
NC_000002.11:g.113875478C>T , CM000664.1:g.113875478C>T GRCh37
NC_000002.10:g.113591949C>T NCBI36
NG_021240.1:g.5009C>T , LRG_188:g.5009C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.-272-2165C>T ENSP00000387210.1:n.-272-2165C>T
ENST00000465812.6:n.775+236C>T
ENST00000259206.9:c.-118C>T ENSP00000259206.5:n.-118C>T
ENST00000354115.6:c.-118C>T ENSP00000329072.3:n.-118C>T
ENST00000361779.7:c.-337C>T ENSP00000354816.3:n.-337C>T
ENST00000409052.5:c.-272-2165C>T ENSP00000387210.1:n.-272-2165C>T
NM_000577.4:c.-118C>T NP_000568.1:n.-118C>T
NM_173841.2:c.-118C>T , LRG_188t1:c.-118C>T NP_776213.1:n.-118C>T
NM_173843.2:c.-337C>T NP_776215.1:n.-337C>T
XM_011511121.1:c.-272-2165C>T XP_011509423.1:n.-272-2165C>T
NM_001318914.1:c.-400C>T NP_001305843.1:n.-400C>T