Canonical Allele Identifier: CA535235086

Gene: IL1RN

Linked Data

• dbSNP Id: rs1436069326
• gnomAD v2: 2-113875588-C-T
• gnomAD v4: 2-113118011-C-T
• MyVariant Identifiers: chr2:g.113875588C>T (hg19) ; chr2:g.113118011C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113118011C>T , CM000664.2:g.113118011C>T	GRCh38
NC_000002.11:g.113875588C>T , CM000664.1:g.113875588C>T	GRCh37
NC_000002.10:g.113592059C>T	NCBI36
NG_021240.1:g.5119C>T , LRG_188:g.5119C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2055C>T	ENSP00000387210.1:n.-272-2055C>T
ENST00000465812.6:n.775+346C>T
ENST00000696881.1:c.-290C>T	ENSP00000512949.1:n.-290C>T
ENST00000259206.9:c.-8C>T	ENSP00000259206.5:n.-8C>T
ENST00000354115.6:c.-8C>T	ENSP00000329072.3:n.-8C>T
ENST00000361779.7:c.-227C>T	ENSP00000354816.3:n.-227C>T
ENST00000409052.5:c.-272-2055C>T	ENSP00000387210.1:n.-272-2055C>T
ENST00000486167.1:n.31C>T
NM_000577.4:c.-8C>T	NP_000568.1:n.-8C>T
NM_173841.2:c.-8C>T , LRG_188t1:c.-8C>T	NP_776213.1:n.-8C>T
NM_173843.2:c.-227C>T	NP_776215.1:n.-227C>T
XM_006712497.2:c.-290C>T	XP_006712560.1:n.-290C>T
XM_011511121.1:c.-272-2055C>T	XP_011509423.1:n.-272-2055C>T
NM_001318914.1:c.-290C>T	NP_001305843.1:n.-290C>T
NM_000577.5:c.-8C>T	NP_000568.1:n.-8C>T
NM_001318914.2:c.-290C>T	NP_001305843.1:n.-290C>T
NM_173843.3:c.-227C>T	NP_776215.1:n.-227C>T
NM_173841.3:c.-8C>T	NP_776213.1:n.-8C>T