Canonical Allele Identifier: CA754317039
Gene: IL18RAP HGNC NCBI

Linked Data

dbSNP Id: rs1433451171

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102444507C>G , CM000664.2:g.102444507C>G GRCh38
NC_000002.11:g.103060967C>G , CM000664.1:g.103060967C>G GRCh37
NC_000002.10:g.102427399C>G NCBI36
NG_011481.1:g.30714C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000687160.1:c.921-682C>G MANE Select ENSP00000510345.1:n.921-682C>G
ENST00000264260.6:c.921-682C>G ENSP00000264260.2:n.921-682C>G
ENST00000409369.1:c.495-682C>G ENSP00000387201.1:n.495-682C>G
NM_003853.3:c.921-682C>G NP_003844.1:n.921-682C>G
XM_011512087.1:c.495-682C>G XP_011510389.1:n.495-682C>G
XM_011512088.1:c.495-682C>G XP_011510390.1:n.495-682C>G
XR_923052.1:n.1352+415C>G
XM_011512087.2:c.495-682C>G XP_011510389.1:n.495-682C>G
XM_011512088.2:c.495-682C>G XP_011510390.1:n.495-682C>G
XM_017005173.1:c.62+415C>G XP_016860662.1:n.62+415C>G
XM_024453197.1:c.921-682C>G XP_024308965.1:n.921-682C>G
XM_024453198.1:c.921-682C>G XP_024308966.1:n.921-682C>G
XM_024453199.1:c.921-682C>G XP_024308967.1:n.921-682C>G
XM_024453200.1:c.921-682C>G XP_024308968.1:n.921-682C>G
XM_024453201.1:c.921-682C>G XP_024308969.1:n.921-682C>G
XR_001739011.2:n.1832+415C>G
NM_001393486.1:c.921-682C>G NP_001380415.1:n.921-682C>G
NM_001393487.1:c.921-682C>G MANE Select NP_001380416.1:n.921-682C>G
NM_001393488.1:c.495-682C>G NP_001380417.1:n.495-682C>G
NM_001393489.1:c.495-682C>G NP_001380418.1:n.495-682C>G
NM_003853.4:c.921-682C>G NP_003844.1:n.921-682C>G