Canonical Allele Identifier: CA755278411

Gene: IL1RN

Linked Data

• dbSNP Id: rs1414989082
• gnomAD v3: 2-113133662-G-T
• gnomAD v4: 2-113133662-G-T
• MyVariant Identifiers: chr2:g.113891239G>T (hg19) ; chr2:g.113133662G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113133662G>T , CM000664.2:g.113133662G>T	GRCh38
NC_000002.11:g.113891239G>T , CM000664.1:g.113891239G>T	GRCh37
NC_000002.10:g.113607710G>T	NCBI36
NG_021240.1:g.20770G>T , LRG_188:g.20770G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.*649G>T	ENSP00000387210.1:n.*649G>T
ENST00000696880.1:c.*328G>T	ENSP00000512948.1:n.*328G>T
ENST00000409930.4:c.*791G>T MANE Select	ENSP00000387173.3:n.*791G>T
ENST00000259206.9:c.*791G>T	ENSP00000259206.5:n.*791G>T
ENST00000354115.6:c.*791G>T	ENSP00000329072.3:n.*791G>T
ENST00000361779.7:c.*791G>T	ENSP00000354816.3:n.*791G>T
ENST00000409052.5:c.*649G>T	ENSP00000387210.1:n.*649G>T
NM_000577.4:c.*791G>T	NP_000568.1:n.*791G>T
NM_173841.2:c.*791G>T , LRG_188t1:c.*791G>T	NP_776213.1:n.*791G>T
NM_173842.2:c.*791G>T	NP_776214.1:n.*791G>T
NM_173843.2:c.*791G>T	NP_776215.1:n.*791G>T
XM_005263661.3:c.*791G>T	XP_005263718.1:n.*791G>T
XM_006712497.2:c.*791G>T	XP_006712560.1:n.*791G>T
XM_011511121.1:c.*791G>T	XP_011509423.1:n.*791G>T
NM_001318914.1:c.*791G>T	NP_001305843.1:n.*791G>T
XM_005263661.4:c.*791G>T	XP_005263718.1:n.*791G>T
NM_000577.5:c.*791G>T	NP_000568.1:n.*791G>T
NM_001318914.2:c.*791G>T	NP_001305843.1:n.*791G>T
NM_173842.3:c.*791G>T MANE Select	NP_776214.1:n.*791G>T
NM_173843.3:c.*791G>T	NP_776215.1:n.*791G>T
NM_001379360.1:c.*791G>T	NP_001366289.1:n.*791G>T
NM_173841.3:c.*791G>T	NP_776213.1:n.*791G>T