Canonical Allele Identifier: CA1275255120
Gene: IL18RAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102419398G= , CM000664.2:g.102419398G= GRCh38
NC_000002.11:g.103035858G= , CM000664.1:g.103035858G= GRCh37
NC_000002.10:g.102402290G= NCBI36
NG_011481.1:g.5605G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264260.6:c.-337-163G= ENSP00000264260.2:n.-337-163G=
NM_003853.3:c.-337-163G= NP_003844.1:n.-337-163G=
XM_011512087.1:c.-438-163G= XP_011510389.1:n.-438-163G=
XM_011512087.2:c.-438-163G= XP_011510389.1:n.-438-163G=
XM_024453197.1:c.-1292-163G= XP_024308965.1:n.-1292-163G=
XM_024453198.1:c.-446-163G= XP_024308966.1:n.-446-163G=
XM_024453199.1:c.-589-163G= XP_024308967.1:n.-589-163G=
XM_024453201.1:c.-101+458G= XP_024308969.1:n.-101+458G=
NM_001393486.1:c.-337-163G= NP_001380415.1:n.-337-163G=
NM_001393488.1:c.-967-163G= NP_001380417.1:n.-967-163G=
NM_001393489.1:c.-438-163G= NP_001380418.1:n.-438-163G=
NM_003853.4:c.-337-163G= NP_003844.1:n.-337-163G=