Canonical Allele Identifier: CA11025319
Gene: IL1RN HGNC NCBI
COSMIC:
COSN6674383 (not active)
MyVariant.info:
GRCh38 chr2:g.113126824G>A
GRCh37 chr2:g.113884401G>A
gnomAD v2:
2:113884401 G / A
gnomAD v3:
2:113126824 G / A
gnomAD v4:
chr2-113126824-G-A
Joint Max Group AF 0.64393524 (EAS)
Genomes Max Group AF 0.64393524 (EAS)
dbSNP:
439154
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113126824G>A , CM000664.2:g.113126824G>A GRCh38
NC_000002.11:g.113884401G>A , CM000664.1:g.113884401G>A GRCh37
NC_000002.10:g.113600872G>A NCBI36
NG_021240.1:g.13932G>A , LRG_188:g.13932G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.-38-865G>A ENSP00000387210.1:n.-38-865G>A
ENST00000696881.1:c.-38-865G>A ENSP00000512949.1:n.-38-865G>A
ENST00000259206.9:c.74-865G>A ENSP00000259206.5:n.74-865G>A
ENST00000354115.6:c.11-865G>A ENSP00000329072.3:n.11-865G>A
ENST00000361779.7:c.-38-865G>A ENSP00000354816.3:n.-38-865G>A
ENST00000409052.5:c.-38-865G>A ENSP00000387210.1:n.-38-865G>A
ENST00000486167.1:n.49-865G>A
NM_000577.4:c.11-865G>A NP_000568.1:n.11-865G>A
NM_173841.2:c.74-865G>A , LRG_188t1:c.74-865G>A NP_776213.1:n.74-865G>A
NM_173843.2:c.-38-865G>A NP_776215.1:n.-38-865G>A
XM_005263661.3:c.-765G>A XP_005263718.1:n.-765G>A
XM_006712497.2:c.-38-865G>A XP_006712560.1:n.-38-865G>A
XM_011511121.1:c.-38-865G>A XP_011509423.1:n.-38-865G>A
NM_001318914.1:c.-38-865G>A NP_001305843.1:n.-38-865G>A
NM_000577.5:c.11-865G>A NP_000568.1:n.11-865G>A
NM_001318914.2:c.-38-865G>A NP_001305843.1:n.-38-865G>A
NM_173843.3:c.-38-865G>A NP_776215.1:n.-38-865G>A
NM_173841.3:c.74-865G>A NP_776213.1:n.74-865G>A
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