Canonical Allele Identifier: CA1275048790

Gene: IL1R2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102000742T= , CM000664.2:g.102000742T=	GRCh38
NC_000002.11:g.102617204T= , CM000664.1:g.102617204T=	GRCh37
NC_000002.10:g.101983636T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332549.8:c.-61-7773T= MANE Select	ENSP00000330959.3:n.-61-7773T=
ENST00000332549.7:c.-61-7773T=	ENSP00000330959.3:n.-61-7773T=
ENST00000393414.6:c.-62+1626T=	ENSP00000377066.2:n.-62+1626T=
ENST00000464994.5:n.75-7773T=
ENST00000493749.1:n.53-7773T=
NM_001261419.1:c.-61-7773T=	NP_001248348.1:n.-61-7773T=
NM_004633.3:c.-61-7773T=	NP_004624.1:n.-61-7773T=
NR_048564.1:n.155+1626T=
XM_006712734.2:c.-61-7773T=	XP_006712797.1:n.-61-7773T=
XM_006712736.2:c.15-7773T=	XP_006712799.1:n.15-7773T=
XM_011511803.1:c.117+1626T=	XP_011510105.1:n.117+1626T=
XM_011511805.1:c.39+419T=	XP_011510107.1:n.39+419T=
XM_006712734.3:c.-61-7773T=	XP_006712797.1:n.-61-7773T=
XM_006712736.3:c.15-7773T=	XP_006712799.1:n.15-7773T=
XM_011511803.2:c.117+1626T=	XP_011510105.1:n.117+1626T=
XM_011511805.3:c.39+419T=	XP_011510107.1:n.39+419T=
XM_017004889.1:c.-189+8731T=	XP_016860378.1:n.-189+8731T=
XM_024453129.1:c.-156-7773T=	XP_024308897.1:n.-156-7773T=
NM_004633.4:c.-61-7773T= MANE Select	NP_004624.1:n.-61-7773T=
NM_001261419.2:c.-61-7773T=	NP_001248348.1:n.-61-7773T=
NR_048564.2:n.156+1626T=