Canonical Allele Identifier: CA755268758

Gene: IL1RN

Linked Data

• dbSNP Id: rs1479479601
• gnomAD v4: 2-113117961-C-G
• MyVariant Identifiers: chr2:g.113875538C>G (hg19) ; chr2:g.113117961C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113117961C>G , CM000664.2:g.113117961C>G	GRCh38
NC_000002.11:g.113875538C>G , CM000664.1:g.113875538C>G	GRCh37
NC_000002.10:g.113592009C>G	NCBI36
NG_021240.1:g.5069C>G , LRG_188:g.5069C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2105C>G	ENSP00000387210.1:n.-272-2105C>G
ENST00000465812.6:n.775+296C>G
ENST00000696881.1:c.-340C>G	ENSP00000512949.1:n.-340C>G
ENST00000259206.9:c.-58C>G	ENSP00000259206.5:n.-58C>G
ENST00000354115.6:c.-58C>G	ENSP00000329072.3:n.-58C>G
ENST00000361779.7:c.-277C>G	ENSP00000354816.3:n.-277C>G
ENST00000409052.5:c.-272-2105C>G	ENSP00000387210.1:n.-272-2105C>G
NM_000577.4:c.-58C>G	NP_000568.1:n.-58C>G
NM_173841.2:c.-58C>G , LRG_188t1:c.-58C>G	NP_776213.1:n.-58C>G
NM_173843.2:c.-277C>G	NP_776215.1:n.-277C>G
XM_011511121.1:c.-272-2105C>G	XP_011509423.1:n.-272-2105C>G
NM_001318914.1:c.-340C>G	NP_001305843.1:n.-340C>G