Canonical Allele Identifier: CA1275063291

Gene: IL1R2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102020381A= , CM000664.2:g.102020381A=	GRCh38
NC_000002.11:g.102636843A= , CM000664.1:g.102636843A=	GRCh37
NC_000002.10:g.102003275A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332549.8:c.688+569A= MANE Select	ENSP00000330959.3:n.688+569A=
ENST00000332549.7:c.688+569A=	ENSP00000330959.3:n.688+569A=
ENST00000393414.6:c.688+569A=	ENSP00000377066.2:n.688+569A=
ENST00000441002.1:c.688+569A=	ENSP00000414611.1:n.688+569A=
NM_001261419.1:c.688+569A=	NP_001248348.1:n.688+569A=
NM_004633.3:c.688+569A=	NP_004624.1:n.688+569A=
NR_048564.1:n.904+569A=
XM_006712734.2:c.688+569A=	XP_006712797.1:n.688+569A=
XM_006712736.2:c.763+569A=	XP_006712799.1:n.763+569A=
XM_011511801.1:c.817+569A=	XP_011510103.1:n.817+569A=
XM_011511802.1:c.817+569A=	XP_011510104.1:n.817+569A=
XM_011511803.1:c.706+569A=	XP_011510105.1:n.706+569A=
XM_011511804.1:c.688+569A=	XP_011510106.1:n.688+569A=
XM_011511805.1:c.628+569A=	XP_011510107.1:n.628+569A=
XM_011511806.1:c.817+569A=	XP_011510108.1:n.817+569A=
XM_011511807.1:c.818-295A=	XP_011510109.1:n.818-295A=
XR_923024.1:n.2562+569A=
XM_006712734.3:c.688+569A=	XP_006712797.1:n.688+569A=
XM_006712736.3:c.763+569A=	XP_006712799.1:n.763+569A=
XM_011511801.2:c.817+569A=	XP_011510103.1:n.817+569A=
XM_011511803.2:c.706+569A=	XP_011510105.1:n.706+569A=
XM_011511804.3:c.688+569A=	XP_011510106.1:n.688+569A=
XM_011511805.3:c.628+569A=	XP_011510107.1:n.628+569A=
XM_017004889.1:c.433+569A=	XP_016860378.1:n.433+569A=
XM_024453129.1:c.433+569A=	XP_024308897.1:n.433+569A=
XR_923024.2:n.3277+569A=
NM_004633.4:c.688+569A= MANE Select	NP_004624.1:n.688+569A=
NM_001261419.2:c.688+569A=	NP_001248348.1:n.688+569A=
NR_048564.2:n.905+569A=