Canonical Allele Identifier: CA52873188

Gene: IL1R2

Linked Data

• dbSNP Id: rs1016147818
• MyVariant Identifiers: chr2:g.102610732C>T (hg19) ; chr2:g.101994270C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101994270C>T , CM000664.2:g.101994270C>T	GRCh38
NC_000002.11:g.102610732C>T , CM000664.1:g.102610732C>T	GRCh37
NC_000002.10:g.101977164C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332549.8:c.-62+2259C>T MANE Select	ENSP00000330959.3:n.-62+2259C>T
ENST00000332549.7:c.-62+2259C>T	ENSP00000330959.3:n.-62+2259C>T
ENST00000464994.5:n.74+2237C>T
ENST00000493749.1:n.52+2259C>T
NM_001261419.1:c.-62+2259C>T	NP_001248348.1:n.-62+2259C>T
NM_004633.3:c.-62+2259C>T	NP_004624.1:n.-62+2259C>T
XM_006712734.2:c.-62+2274C>T	XP_006712797.1:n.-62+2274C>T
XM_006712736.2:c.14+2237C>T	XP_006712799.1:n.14+2237C>T
XM_006712734.3:c.-62+2274C>T	XP_006712797.1:n.-62+2274C>T
XM_006712736.3:c.14+2237C>T	XP_006712799.1:n.14+2237C>T
XM_017004889.1:c.-189+2259C>T	XP_016860378.1:n.-189+2259C>T
XM_024453129.1:c.-157+2274C>T	XP_024308897.1:n.-157+2274C>T
NM_004633.4:c.-62+2259C>T MANE Select	NP_004624.1:n.-62+2259C>T
NM_001261419.2:c.-62+2259C>T	NP_001248348.1:n.-62+2259C>T