Canonical Allele Identifier: CA755268885

Gene: IL1RN

Linked Data

• dbSNP Id: rs1209498379
• gnomAD v4: 2-113118077-A-G
• MyVariant Identifiers: chr2:g.113875654A>G (hg19) ; chr2:g.113118077A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113118077A>G , CM000664.2:g.113118077A>G	GRCh38
NC_000002.11:g.113875654A>G , CM000664.1:g.113875654A>G	GRCh37
NC_000002.10:g.113592125A>G	NCBI36
NG_021240.1:g.5185A>G , LRG_188:g.5185A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-1989A>G	ENSP00000387210.1:n.-272-1989A>G
ENST00000465812.6:n.775+412A>G
ENST00000696881.1:c.-273+49A>G	ENSP00000512949.1:n.-273+49A>G
ENST00000259206.9:c.10+49A>G	ENSP00000259206.5:n.10+49A>G
ENST00000354115.6:c.10+49A>G	ENSP00000329072.3:n.10+49A>G
ENST00000361779.7:c.-210+49A>G	ENSP00000354816.3:n.-210+49A>G
ENST00000409052.5:c.-272-1989A>G	ENSP00000387210.1:n.-272-1989A>G
ENST00000486167.1:n.48+49A>G
NM_000577.4:c.10+49A>G	NP_000568.1:n.10+49A>G
NM_173841.2:c.10+49A>G , LRG_188t1:c.10+49A>G	NP_776213.1:n.10+49A>G
NM_173843.2:c.-210+49A>G	NP_776215.1:n.-210+49A>G
XM_006712497.2:c.-273+49A>G	XP_006712560.1:n.-273+49A>G
XM_011511121.1:c.-272-1989A>G	XP_011509423.1:n.-272-1989A>G
NM_001318914.1:c.-273+49A>G	NP_001305843.1:n.-273+49A>G
NM_000577.5:c.10+49A>G	NP_000568.1:n.10+49A>G
NM_001318914.2:c.-273+49A>G	NP_001305843.1:n.-273+49A>G
NM_173843.3:c.-210+49A>G	NP_776215.1:n.-210+49A>G
NM_173841.3:c.10+49A>G	NP_776213.1:n.10+49A>G