Canonical Allele Identifier: CA2660478156

Gene: IL18RAP

Linked Data

• gnomAD v4: 2-102419450-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419450C>A , CM000664.2:g.102419450C>A	GRCh38
NC_000002.11:g.103035910C>A , CM000664.1:g.103035910C>A	GRCh37
NC_000002.10:g.102402342C>A	NCBI36
NG_011481.1:g.5657C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264260.6:c.-337-111C>A	ENSP00000264260.2:n.-337-111C>A
ENST00000450855.1:c.-448C>A	ENSP00000389815.1:n.-448C>A
NM_003853.3:c.-337-111C>A	NP_003844.1:n.-337-111C>A
XM_011512087.1:c.-438-111C>A	XP_011510389.1:n.-438-111C>A
XM_011512087.2:c.-438-111C>A	XP_011510389.1:n.-438-111C>A
XM_024453197.1:c.-1292-111C>A	XP_024308965.1:n.-1292-111C>A
XM_024453198.1:c.-446-111C>A	XP_024308966.1:n.-446-111C>A
XM_024453199.1:c.-589-111C>A	XP_024308967.1:n.-589-111C>A
XM_024453201.1:c.-101+510C>A	XP_024308969.1:n.-101+510C>A
NM_001393486.1:c.-337-111C>A	NP_001380415.1:n.-337-111C>A
NM_001393488.1:c.-967-111C>A	NP_001380417.1:n.-967-111C>A
NM_001393489.1:c.-438-111C>A	NP_001380418.1:n.-438-111C>A
NM_003853.4:c.-337-111C>A	NP_003844.1:n.-337-111C>A