Canonical Allele Identifier: CA10611865
Gene: IL1RN HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 330845
ClinVar RCV Id: RCV000355397
dbSNP Id: rs9005

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113133835G>A , CM000664.2:g.113133835G>A GRCh38
NC_000002.11:g.113891412G>A , CM000664.1:g.113891412G>A GRCh37
NC_000002.10:g.113607883G>A NCBI36
NG_021240.1:g.20943G>A , LRG_188:g.20943G>A

Transcript Alleles

HGVS Amino-acid change
NM_000577.4:c.*964G>A VV NP_000568.1:p.=
NM_173841.2:c.*964G>A , LRG_188t1:c.*964G>A NP_776213.1:p.=
NM_173842.2:c.*964G>A VV NP_776214.1:p.=
NM_173843.2:c.*964G>A VV NP_776215.1:p.=
XM_005263661.3:c.*964G>A XP_005263718.1:p.=
XM_006712497.2:c.*964G>A XP_006712560.1:p.=
XM_011511121.1:c.*964G>A XP_011509423.1:p.=
NM_001318914.1:c.*964G>A VV NP_001305843.1:p.=
XM_005263661.4:c.*964G>A XP_005263718.1:p.=
ENST00000259206.9:c.*964G>A ENSP00000259206.5:p.=
ENST00000354115.6:c.*964G>A ENSP00000329072.3:p.=
ENST00000361779.7:c.*964G>A ENSP00000354816.3:p.=
ENST00000409052.5:c.*822G>A ENSP00000387210.1:p.=