Canonical Allele Identifier: CA11022338
Gene: IL1R2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102026557A>G , CM000664.2:g.102026557A>G GRCh38
NC_000002.11:g.102643019A>G , CM000664.1:g.102643019A>G GRCh37
NC_000002.10:g.102009451A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000332549.8:c.1030+304A>G MANE Select ENSP00000330959.3:n.1030+304A>G
ENST00000332549.7:c.1030+304A>G ENSP00000330959.3:n.1030+304A>G
ENST00000393414.6:c.1030+304A>G ENSP00000377066.2:n.1030+304A>G
ENST00000474085.5:n.466+304A>G
ENST00000485335.1:n.511+304A>G
NM_004633.3:c.1030+304A>G NP_004624.1:n.1030+304A>G
NR_048564.1:n.1246+304A>G
XM_006712734.2:c.1030+304A>G XP_006712797.1:n.1030+304A>G
XM_006712736.2:c.1105+304A>G XP_006712799.1:n.1105+304A>G
XM_011511801.1:c.1159+304A>G XP_011510103.1:n.1159+304A>G
XM_011511802.1:c.1096+304A>G XP_011510104.1:n.1096+304A>G
XM_011511803.1:c.1048+304A>G XP_011510105.1:n.1048+304A>G
XM_011511804.1:c.1030+304A>G XP_011510106.1:n.1030+304A>G
XM_011511805.1:c.970+304A>G XP_011510107.1:n.970+304A>G
XM_011511808.1:c.544+304A>G XP_011510110.1:n.544+304A>G
XM_006712734.3:c.1030+304A>G XP_006712797.1:n.1030+304A>G
XM_006712736.3:c.1105+304A>G XP_006712799.1:n.1105+304A>G
XM_011511801.2:c.1159+304A>G XP_011510103.1:n.1159+304A>G
XM_011511803.2:c.1048+304A>G XP_011510105.1:n.1048+304A>G
XM_011511804.3:c.1030+304A>G XP_011510106.1:n.1030+304A>G
XM_011511805.3:c.970+304A>G XP_011510107.1:n.970+304A>G
XM_011511808.2:c.544+304A>G XP_011510110.1:n.544+304A>G
XM_017004889.1:c.775+304A>G XP_016860378.1:n.775+304A>G
XM_024453129.1:c.775+304A>G XP_024308897.1:n.775+304A>G
NM_004633.4:c.1030+304A>G MANE Select NP_004624.1:n.1030+304A>G
NR_048564.2:n.1247+304A>G
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