Canonical Allele Identifier: CA10610618

Gene: IL1RN

Linked Data

• ClinVar Variation Id: 330837
• ClinVar RCV Id: RCV000394829
• dbSNP Id: rs4252028
• gnomAD v2: 2-113890759-G-A
• gnomAD v3: 2-113133182-G-A
• gnomAD v4: 2-113133182-G-A
• MyVariant Identifiers: chr2:g.113890759G>A (hg19) ; chr2:g.113133182G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113133182G>A , CM000664.2:g.113133182G>A	GRCh38
NC_000002.11:g.113890759G>A , CM000664.1:g.113890759G>A	GRCh37
NC_000002.10:g.113607230G>A	NCBI36
NG_021240.1:g.20290G>A , LRG_188:g.20290G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.*311G>A	ENSP00000387210.1:n.*311G>A
ENST00000696879.1:c.*311G>A	ENSP00000512947.1:n.*311G>A
ENST00000696880.1:c.*211+100G>A	ENSP00000512948.1:n.*211+100G>A
ENST00000696882.1:c.*615G>A	ENSP00000512950.1:n.*615G>A
ENST00000409930.4:c.*311G>A MANE Select	ENSP00000387173.3:n.*311G>A
ENST00000259206.9:c.*311G>A	ENSP00000259206.5:n.*311G>A
ENST00000354115.6:c.*311G>A	ENSP00000329072.3:n.*311G>A
ENST00000361779.7:c.*311G>A	ENSP00000354816.3:n.*311G>A
ENST00000409052.5:c.*311G>A	ENSP00000387210.1:n.*311G>A
NM_000577.4:c.*311G>A	NP_000568.1:n.*311G>A
NM_173841.2:c.*311G>A , LRG_188t1:c.*311G>A	NP_776213.1:n.*311G>A
NM_173842.2:c.*311G>A	NP_776214.1:n.*311G>A
NM_173843.2:c.*311G>A	NP_776215.1:n.*311G>A
XM_005263661.3:c.*311G>A	XP_005263718.1:n.*311G>A
XM_006712497.2:c.*311G>A	XP_006712560.1:n.*311G>A
XM_011511121.1:c.*311G>A	XP_011509423.1:n.*311G>A
NM_001318914.1:c.*311G>A	NP_001305843.1:n.*311G>A
XM_005263661.4:c.*311G>A	XP_005263718.1:n.*311G>A
NM_000577.5:c.*311G>A	NP_000568.1:n.*311G>A
NM_001318914.2:c.*311G>A	NP_001305843.1:n.*311G>A
NM_173842.3:c.*311G>A MANE Select	NP_776214.1:n.*311G>A
NM_173843.3:c.*311G>A	NP_776215.1:n.*311G>A
NM_001379360.1:c.*311G>A	NP_001366289.1:n.*311G>A
NM_173841.3:c.*311G>A	NP_776213.1:n.*311G>A