Canonical Allele Identifier: CA1034379704
Gene: IL18RAP HGNC NCBI

Linked Data

dbSNP Id: rs1681424122

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102419245C>A , CM000664.2:g.102419245C>A GRCh38
NC_000002.11:g.103035705C>A , CM000664.1:g.103035705C>A GRCh37
NC_000002.10:g.102402137C>A NCBI36
NG_011481.1:g.5452C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264260.6:c.-338+305C>A ENSP00000264260.2:n.-338+305C>A
NM_003853.3:c.-338+305C>A NP_003844.1:n.-338+305C>A
XM_011512087.1:c.-439+305C>A XP_011510389.1:n.-439+305C>A
XM_011512087.2:c.-439+305C>A XP_011510389.1:n.-439+305C>A
XM_024453197.1:c.-1293+305C>A XP_024308965.1:n.-1293+305C>A
XM_024453198.1:c.-447+305C>A XP_024308966.1:n.-447+305C>A
XM_024453199.1:c.-590+305C>A XP_024308967.1:n.-590+305C>A
XM_024453201.1:c.-101+305C>A XP_024308969.1:n.-101+305C>A
NM_001393486.1:c.-338+305C>A NP_001380415.1:n.-338+305C>A
NM_001393488.1:c.-968+305C>A NP_001380417.1:n.-968+305C>A
NM_001393489.1:c.-439+305C>A NP_001380418.1:n.-439+305C>A
NM_003853.4:c.-338+305C>A NP_003844.1:n.-338+305C>A