Canonical Allele Identifier: CA1275058002

Gene: IL1R2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102009418T>C , CM000664.2:g.102009418T>C	GRCh38
NC_000002.11:g.102625880T>C , CM000664.1:g.102625880T>C	GRCh37
NC_000002.10:g.101992312T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332549.8:c.68-144T>C MANE Select	ENSP00000330959.3:n.68-144T>C
ENST00000332549.7:c.68-144T>C	ENSP00000330959.3:n.68-144T>C
ENST00000393414.6:c.68-144T>C	ENSP00000377066.2:n.68-144T>C
ENST00000441002.1:c.68-144T>C	ENSP00000414611.1:n.68-144T>C
ENST00000457817.5:c.68-144T>C	ENSP00000408415.1:n.68-144T>C
ENST00000464994.5:n.203-144T>C
ENST00000493749.1:n.181-144T>C
NM_001261419.1:c.68-144T>C	NP_001248348.1:n.68-144T>C
NM_004633.3:c.68-144T>C	NP_004624.1:n.68-144T>C
NR_048564.1:n.284-144T>C
XM_006712734.2:c.68-144T>C	XP_006712797.1:n.68-144T>C
XM_006712736.2:c.143-144T>C	XP_006712799.1:n.143-144T>C
XM_011511801.1:c.197-144T>C	XP_011510103.1:n.197-144T>C
XM_011511802.1:c.197-144T>C	XP_011510104.1:n.197-144T>C
XM_011511803.1:c.246-304T>C	XP_011510105.1:n.246-304T>C
XM_011511804.1:c.68-144T>C	XP_011510106.1:n.68-144T>C
XM_011511805.1:c.168-304T>C	XP_011510107.1:n.168-304T>C
XM_011511806.1:c.197-144T>C	XP_011510108.1:n.197-144T>C
XM_011511807.1:c.197-144T>C	XP_011510109.1:n.197-144T>C
XR_923024.1:n.1942-144T>C
XM_006712734.3:c.68-144T>C	XP_006712797.1:n.68-144T>C
XM_006712736.3:c.143-144T>C	XP_006712799.1:n.143-144T>C
XM_011511801.2:c.197-144T>C	XP_011510103.1:n.197-144T>C
XM_011511803.2:c.246-304T>C	XP_011510105.1:n.246-304T>C
XM_011511804.3:c.68-144T>C	XP_011510106.1:n.68-144T>C
XM_011511805.3:c.168-304T>C	XP_011510107.1:n.168-304T>C
XM_017004889.1:c.-188-144T>C	XP_016860378.1:n.-188-144T>C
XM_024453129.1:c.-28-304T>C	XP_024308897.1:n.-28-304T>C
XR_923024.2:n.2657-144T>C
NM_004633.4:c.68-144T>C MANE Select	NP_004624.1:n.68-144T>C
NM_001261419.2:c.68-144T>C	NP_001248348.1:n.68-144T>C
NR_048564.2:n.285-144T>C