Canonical Allele Identifier: CA11022328

Gene: IL1R2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102005914A>G , CM000664.2:g.102005914A>G	GRCh38
NC_000002.11:g.102622376A>G , CM000664.1:g.102622376A>G	GRCh37
NC_000002.10:g.101988808A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004633.4:c.-61-2601A>G MANE Select	NP_004624.1:n.-61-2601A>G
ENST00000332549.8:c.-61-2601A>G MANE Select	ENSP00000330959.3:n.-61-2601A>G
NM_001261419.1:c.-61-2601A>G	NP_001248348.1:n.-61-2601A>G
NM_001261419.2:c.-61-2601A>G	NP_001248348.1:n.-61-2601A>G
NM_004633.3:c.-61-2601A>G	NP_004624.1:n.-61-2601A>G
NR_048564.1:n.156-2601A>G
NR_048564.2:n.157-2601A>G
ENST00000332549.7:c.-61-2601A>G	ENSP00000330959.3:n.-61-2601A>G
ENST00000393414.6:c.-61-2601A>G	ENSP00000377066.2:n.-61-2601A>G
ENST00000457817.5:c.-61-2601A>G	ENSP00000408415.1:n.-61-2601A>G
ENST00000464994.5:n.75-2601A>G
ENST00000493749.1:n.53-2601A>G
XM_006712734.2:c.-61-2601A>G	XP_006712797.1:n.-61-2601A>G
XM_006712734.3:c.-61-2601A>G	XP_006712797.1:n.-61-2601A>G
XM_006712736.2:c.15-2601A>G	XP_006712799.1:n.15-2601A>G
XM_006712736.3:c.15-2601A>G	XP_006712799.1:n.15-2601A>G
XM_011511801.1:c.-611A>G	XP_011510103.1:n.-611A>G
XM_011511801.2:c.-611A>G	XP_011510103.1:n.-611A>G
XM_011511802.1:c.-611A>G	XP_011510104.1:n.-611A>G
XM_011511803.1:c.118-2601A>G	XP_011510105.1:n.118-2601A>G
XM_011511803.2:c.118-2601A>G	XP_011510105.1:n.118-2601A>G
XM_011511804.1:c.-61-2601A>G	XP_011510106.1:n.-61-2601A>G
XM_011511804.3:c.-61-2601A>G	XP_011510106.1:n.-61-2601A>G
XM_011511805.1:c.40-2601A>G	XP_011510107.1:n.40-2601A>G
XM_011511805.3:c.40-2601A>G	XP_011510107.1:n.40-2601A>G
XM_011511806.1:c.-611A>G	XP_011510108.1:n.-611A>G
XM_011511807.1:c.-611A>G	XP_011510109.1:n.-611A>G
XM_017004889.1:c.-188-3648A>G	XP_016860378.1:n.-188-3648A>G
XM_024453129.1:c.-156-2601A>G	XP_024308897.1:n.-156-2601A>G
XR_923024.1:n.1135A>G
XR_923024.2:n.1850A>G