Canonical Allele Identifier: CA53698153

Gene: IL1RN

Linked Data

• ClinVar Variation Id: 893932
• ClinVar RCV Id: RCV001133237
• dbSNP Id: rs4252026
• gnomAD v2: 2-113890523-C-G
• gnomAD v3: 2-113132946-C-G
• gnomAD v4: 2-113132946-C-G
• MyVariant Identifiers: chr2:g.113890523C>G (hg19) ; chr2:g.113132946C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132946C>G , CM000664.2:g.113132946C>G	GRCh38
NC_000002.11:g.113890523C>G , CM000664.1:g.113890523C>G	GRCh37
NC_000002.10:g.113606994C>G	NCBI36
NG_021240.1:g.20054C>G , LRG_188:g.20054C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409052.6:c.*75C>G	ENSP00000387210.1:n.*75C>G
ENST00000696879.1:c.*75C>G	ENSP00000512947.1:n.*75C>G
ENST00000696880.1:c.*75C>G	ENSP00000512948.1:n.*75C>G
ENST00000696881.1:c.*75C>G	ENSP00000512949.1:n.*75C>G
ENST00000696882.1:c.*379C>G	ENSP00000512950.1:n.*379C>G
ENST00000409930.4:c.*75C>G MANE Select	ENSP00000387173.3:n.*75C>G
ENST00000259206.9:c.*75C>G	ENSP00000259206.5:n.*75C>G
ENST00000354115.6:c.*75C>G	ENSP00000329072.3:n.*75C>G
ENST00000361779.7:c.*75C>G	ENSP00000354816.3:n.*75C>G
ENST00000409052.5:c.*75C>G	ENSP00000387210.1:n.*75C>G
ENST00000409930.3:c.*75C>G	ENSP00000387173.3:n.*75C>G
NM_000577.4:c.*75C>G	NP_000568.1:n.*75C>G
NM_173841.2:c.*75C>G , LRG_188t1:c.*75C>G	NP_776213.1:n.*75C>G
NM_173842.2:c.*75C>G	NP_776214.1:n.*75C>G
NM_173843.2:c.*75C>G	NP_776215.1:n.*75C>G
XM_005263661.3:c.*75C>G	XP_005263718.1:n.*75C>G
XM_006712497.2:c.*75C>G	XP_006712560.1:n.*75C>G
XM_011511121.1:c.*75C>G	XP_011509423.1:n.*75C>G
NM_001318914.1:c.*75C>G	NP_001305843.1:n.*75C>G
XM_005263661.4:c.*75C>G	XP_005263718.1:n.*75C>G
NM_000577.5:c.*75C>G	NP_000568.1:n.*75C>G
NM_001318914.2:c.*75C>G	NP_001305843.1:n.*75C>G
NM_173842.3:c.*75C>G MANE Select	NP_776214.1:n.*75C>G
NM_173843.3:c.*75C>G	NP_776215.1:n.*75C>G
NM_001379360.1:c.*75C>G	NP_001366289.1:n.*75C>G
NM_173841.3:c.*75C>G	NP_776213.1:n.*75C>G