Canonical Allele Identifier: CA428554690
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs1460641135

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113132853C>T , CM000664.2:g.113132853C>T GRCh38
NC_000002.11:g.113890430C>T , CM000664.1:g.113890430C>T GRCh37
NC_000002.10:g.113606901C>T NCBI36
NG_021240.1:g.19961C>T , LRG_188:g.19961C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.414C>T ENSP00000387210.1:p.Tyr138=
ENST00000696879.1:c.414C>T ENSP00000512947.1:p.Tyr138=
ENST00000696880.1:c.414C>T ENSP00000512948.1:p.Tyr138=
ENST00000696881.1:c.414C>T ENSP00000512949.1:p.Tyr138=
ENST00000696882.1:c.*286C>T ENSP00000512950.1:n.*286C>T
ENST00000696883.1:n.461C>T
ENST00000409930.4:c.516C>T MANE Select ENSP00000387173.3:p.Tyr172=
ENST00000259206.9:c.525C>T ENSP00000259206.5:p.Tyr175=
ENST00000354115.6:c.462C>T ENSP00000329072.3:p.Tyr154=
ENST00000361779.7:c.414C>T ENSP00000354816.3:p.Tyr138=
ENST00000409052.5:c.414C>T ENSP00000387210.1:p.Tyr138=
ENST00000409930.3:c.516C>T ENSP00000387173.3:p.Tyr172=
NM_000577.4:c.462C>T NP_000568.1:p.Tyr154=
NM_173841.2:c.525C>T , LRG_188t1:c.525C>T NP_776213.1:p.Tyr175=
NM_173842.2:c.516C>T NP_776214.1:p.Tyr172=
NM_173843.2:c.414C>T NP_776215.1:p.Tyr138=
XM_005263661.3:c.414C>T XP_005263718.1:p.Tyr138=
XM_006712497.2:c.414C>T XP_006712560.1:p.Tyr138=
XM_011511121.1:c.414C>T XP_011509423.1:p.Tyr138=
NM_001318914.1:c.414C>T NP_001305843.1:p.Tyr138=
XM_005263661.4:c.414C>T XP_005263718.1:p.Tyr138=
NM_000577.5:c.462C>T NP_000568.1:p.Tyr154=
NM_001318914.2:c.414C>T NP_001305843.1:p.Tyr138=
NM_173842.3:c.516C>T MANE Select NP_776214.1:p.Tyr172=
NM_173843.3:c.414C>T NP_776215.1:p.Tyr138=
NM_001379360.1:c.414C>T NP_001366289.1:p.Tyr138=
NM_173841.3:c.525C>T NP_776213.1:p.Tyr175=