Canonical Allele Identifier: CA2602760279

Gene: IL18RAP

Linked Data

• dbSNP Id: rs2104272797
• gnomAD v3: 2-102419408-T-C
• gnomAD v4: 2-102419408-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419408T>C , CM000664.2:g.102419408T>C	GRCh38
NC_000002.11:g.103035868T>C , CM000664.1:g.103035868T>C	GRCh37
NC_000002.10:g.102402300T>C	NCBI36
NG_011481.1:g.5615T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264260.6:c.-337-153T>C	ENSP00000264260.2:n.-337-153T>C
NM_003853.3:c.-337-153T>C	NP_003844.1:n.-337-153T>C
XM_011512087.1:c.-438-153T>C	XP_011510389.1:n.-438-153T>C
XM_011512087.2:c.-438-153T>C	XP_011510389.1:n.-438-153T>C
XM_024453197.1:c.-1292-153T>C	XP_024308965.1:n.-1292-153T>C
XM_024453198.1:c.-446-153T>C	XP_024308966.1:n.-446-153T>C
XM_024453199.1:c.-589-153T>C	XP_024308967.1:n.-589-153T>C
XM_024453201.1:c.-101+468T>C	XP_024308969.1:n.-101+468T>C
NM_001393486.1:c.-337-153T>C	NP_001380415.1:n.-337-153T>C
NM_001393488.1:c.-967-153T>C	NP_001380417.1:n.-967-153T>C
NM_001393489.1:c.-438-153T>C	NP_001380418.1:n.-438-153T>C
NM_003853.4:c.-337-153T>C	NP_003844.1:n.-337-153T>C