Canonical Allele Identifier: CA10611832

Gene: IL1RN

Linked Data

• ClinVar Variation Id: 330817
• ClinVar RCV Id: RCV003401348 ; RCV000402395 ; RCV001613074
• dbSNP Id: rs2234677
• gnomAD v2: 2-113875509-G-A
• gnomAD v3: 2-113117932-G-A
• gnomAD v4: 2-113117932-G-A
• MyVariant Identifiers: chr2:g.113875509G>A (hg19) ; chr2:g.113117932G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113117932G>A , CM000664.2:g.113117932G>A	GRCh38
NC_000002.11:g.113875509G>A , CM000664.1:g.113875509G>A	GRCh37
NC_000002.10:g.113591980G>A	NCBI36
NG_021240.1:g.5040G>A , LRG_188:g.5040G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2134G>A	ENSP00000387210.1:n.-272-2134G>A
ENST00000465812.6:n.775+267G>A
ENST00000259206.9:c.-87G>A	ENSP00000259206.5:n.-87G>A
ENST00000354115.6:c.-87G>A	ENSP00000329072.3:n.-87G>A
ENST00000361779.7:c.-306G>A	ENSP00000354816.3:n.-306G>A
ENST00000409052.5:c.-272-2134G>A	ENSP00000387210.1:n.-272-2134G>A
NM_000577.4:c.-87G>A	NP_000568.1:n.-87G>A
NM_173841.2:c.-87G>A , LRG_188t1:c.-87G>A	NP_776213.1:n.-87G>A
NM_173843.2:c.-306G>A	NP_776215.1:n.-306G>A
XM_011511121.1:c.-272-2134G>A	XP_011509423.1:n.-272-2134G>A
NM_001318914.1:c.-369G>A	NP_001305843.1:n.-369G>A