Canonical Allele Identifier: CA2660763958
Gene: IL1RN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113117971A>G , CM000664.2:g.113117971A>G GRCh38
NC_000002.11:g.113875548A>G , CM000664.1:g.113875548A>G GRCh37
NC_000002.10:g.113592019A>G NCBI36
NG_021240.1:g.5079A>G , LRG_188:g.5079A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.-272-2095A>G ENSP00000387210.1:n.-272-2095A>G
ENST00000465812.6:n.775+306A>G
ENST00000696881.1:c.-330A>G ENSP00000512949.1:n.-330A>G
ENST00000259206.9:c.-48A>G ENSP00000259206.5:n.-48A>G
ENST00000354115.6:c.-48A>G ENSP00000329072.3:n.-48A>G
ENST00000361779.7:c.-267A>G ENSP00000354816.3:n.-267A>G
ENST00000409052.5:c.-272-2095A>G ENSP00000387210.1:n.-272-2095A>G
NM_000577.4:c.-48A>G NP_000568.1:n.-48A>G
NM_173841.2:c.-48A>G , LRG_188t1:c.-48A>G NP_776213.1:n.-48A>G
NM_173843.2:c.-267A>G NP_776215.1:n.-267A>G
XM_011511121.1:c.-272-2095A>G XP_011509423.1:n.-272-2095A>G
NM_001318914.1:c.-330A>G NP_001305843.1:n.-330A>G
NM_000577.5:c.-48A>G NP_000568.1:n.-48A>G
NM_001318914.2:c.-330A>G NP_001305843.1:n.-330A>G
NM_173843.3:c.-267A>G NP_776215.1:n.-267A>G
NM_173841.3:c.-48A>G NP_776213.1:n.-48A>G