Canonical Allele Identifier: CA1275055538

Gene: IL1R2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101994296T= , CM000664.2:g.101994296T=	GRCh38
NC_000002.11:g.102610758T= , CM000664.1:g.102610758T=	GRCh37
NC_000002.10:g.101977190T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332549.8:c.-62+2285T= MANE Select	ENSP00000330959.3:n.-62+2285T=
ENST00000332549.7:c.-62+2285T=	ENSP00000330959.3:n.-62+2285T=
ENST00000464994.5:n.74+2263T=
ENST00000493749.1:n.52+2285T=
NM_001261419.1:c.-62+2285T=	NP_001248348.1:n.-62+2285T=
NM_004633.3:c.-62+2285T=	NP_004624.1:n.-62+2285T=
XM_006712734.2:c.-62+2300T=	XP_006712797.1:n.-62+2300T=
XM_006712736.2:c.14+2263T=	XP_006712799.1:n.14+2263T=
XM_006712734.3:c.-62+2300T=	XP_006712797.1:n.-62+2300T=
XM_006712736.3:c.14+2263T=	XP_006712799.1:n.14+2263T=
XM_017004889.1:c.-189+2285T=	XP_016860378.1:n.-189+2285T=
XM_024453129.1:c.-157+2300T=	XP_024308897.1:n.-157+2300T=
NM_004633.4:c.-62+2285T= MANE Select	NP_004624.1:n.-62+2285T=
NM_001261419.2:c.-62+2285T=	NP_001248348.1:n.-62+2285T=