Canonical Allele Identifier: CA1280066388
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs1686633440

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113117923C>A , CM000664.2:g.113117923C>A GRCh38
NC_000002.11:g.113875500C>A , CM000664.1:g.113875500C>A GRCh37
NC_000002.10:g.113591971C>A NCBI36
NG_021240.1:g.5031C>A , LRG_188:g.5031C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.-272-2143C>A ENSP00000387210.1:n.-272-2143C>A
ENST00000465812.6:n.775+258C>A
ENST00000259206.9:c.-96C>A ENSP00000259206.5:n.-96C>A
ENST00000354115.6:c.-96C>A ENSP00000329072.3:n.-96C>A
ENST00000361779.7:c.-315C>A ENSP00000354816.3:n.-315C>A
ENST00000409052.5:c.-272-2143C>A ENSP00000387210.1:n.-272-2143C>A
NM_000577.4:c.-96C>A NP_000568.1:n.-96C>A
NM_173841.2:c.-96C>A , LRG_188t1:c.-96C>A NP_776213.1:n.-96C>A
NM_173843.2:c.-315C>A NP_776215.1:n.-315C>A
XM_011511121.1:c.-272-2143C>A XP_011509423.1:n.-272-2143C>A
NM_001318914.1:c.-378C>A NP_001305843.1:n.-378C>A