Canonical Allele Identifier: CA1034379706

Gene: IL18RAP

Linked Data

• dbSNP Id: rs962034216
• gnomAD v3: 2-102419246-T-C
• gnomAD v4: 2-102419246-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419246T>C , CM000664.2:g.102419246T>C	GRCh38
NC_000002.11:g.103035706T>C , CM000664.1:g.103035706T>C	GRCh37
NC_000002.10:g.102402138T>C	NCBI36
NG_011481.1:g.5453T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264260.6:c.-338+306T>C	ENSP00000264260.2:n.-338+306T>C
NM_003853.3:c.-338+306T>C	NP_003844.1:n.-338+306T>C
XM_011512087.1:c.-439+306T>C	XP_011510389.1:n.-439+306T>C
XM_011512087.2:c.-439+306T>C	XP_011510389.1:n.-439+306T>C
XM_024453197.1:c.-1293+306T>C	XP_024308965.1:n.-1293+306T>C
XM_024453198.1:c.-447+306T>C	XP_024308966.1:n.-447+306T>C
XM_024453199.1:c.-590+306T>C	XP_024308967.1:n.-590+306T>C
XM_024453201.1:c.-101+306T>C	XP_024308969.1:n.-101+306T>C
NM_001393486.1:c.-338+306T>C	NP_001380415.1:n.-338+306T>C
NM_001393488.1:c.-968+306T>C	NP_001380417.1:n.-968+306T>C
NM_001393489.1:c.-439+306T>C	NP_001380418.1:n.-439+306T>C
NM_003853.4:c.-338+306T>C	NP_003844.1:n.-338+306T>C