Canonical Allele Identifier: CA1034368308

Gene: IL1R2

Linked Data

• dbSNP Id: rs1677307598
• gnomAD v3: 2-102020472-T-C
• gnomAD v4: 2-102020472-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102020472T>C , CM000664.2:g.102020472T>C	GRCh38
NC_000002.11:g.102636934T>C , CM000664.1:g.102636934T>C	GRCh37
NC_000002.10:g.102003366T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332549.8:c.688+660T>C MANE Select	ENSP00000330959.3:n.688+660T>C
ENST00000332549.7:c.688+660T>C	ENSP00000330959.3:n.688+660T>C
ENST00000393414.6:c.688+660T>C	ENSP00000377066.2:n.688+660T>C
ENST00000441002.1:c.688+660T>C	ENSP00000414611.1:n.688+660T>C
NM_001261419.1:c.688+660T>C	NP_001248348.1:n.688+660T>C
NM_004633.3:c.688+660T>C	NP_004624.1:n.688+660T>C
NR_048564.1:n.904+660T>C
XM_006712734.2:c.688+660T>C	XP_006712797.1:n.688+660T>C
XM_006712736.2:c.763+660T>C	XP_006712799.1:n.763+660T>C
XM_011511801.1:c.817+660T>C	XP_011510103.1:n.817+660T>C
XM_011511802.1:c.817+660T>C	XP_011510104.1:n.817+660T>C
XM_011511803.1:c.706+660T>C	XP_011510105.1:n.706+660T>C
XM_011511804.1:c.688+660T>C	XP_011510106.1:n.688+660T>C
XM_011511805.1:c.628+660T>C	XP_011510107.1:n.628+660T>C
XM_011511806.1:c.817+660T>C	XP_011510108.1:n.817+660T>C
XM_011511807.1:c.818-204T>C	XP_011510109.1:n.818-204T>C
XR_923024.1:n.2562+660T>C
XM_006712734.3:c.688+660T>C	XP_006712797.1:n.688+660T>C
XM_006712736.3:c.763+660T>C	XP_006712799.1:n.763+660T>C
XM_011511801.2:c.817+660T>C	XP_011510103.1:n.817+660T>C
XM_011511803.2:c.706+660T>C	XP_011510105.1:n.706+660T>C
XM_011511804.3:c.688+660T>C	XP_011510106.1:n.688+660T>C
XM_011511805.3:c.628+660T>C	XP_011510107.1:n.628+660T>C
XM_017004889.1:c.433+660T>C	XP_016860378.1:n.433+660T>C
XM_024453129.1:c.433+660T>C	XP_024308897.1:n.433+660T>C
XR_923024.2:n.3277+660T>C
NM_004633.4:c.688+660T>C MANE Select	NP_004624.1:n.688+660T>C
NM_001261419.2:c.688+660T>C	NP_001248348.1:n.688+660T>C
NR_048564.2:n.905+660T>C