Canonical Allele Identifier: CA754321650

Gene: IL18RAP

Linked Data

• dbSNP Id: rs1278151468
• MyVariant Identifiers: chr2:g.103035826A>G (hg19) ; chr2:g.102419366A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419366A>G , CM000664.2:g.102419366A>G	GRCh38
NC_000002.11:g.103035826A>G , CM000664.1:g.103035826A>G	GRCh37
NC_000002.10:g.102402258A>G	NCBI36
NG_011481.1:g.5573A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264260.6:c.-337-195A>G	ENSP00000264260.2:n.-337-195A>G
NM_003853.3:c.-337-195A>G	NP_003844.1:n.-337-195A>G
XM_011512087.1:c.-438-195A>G	XP_011510389.1:n.-438-195A>G
XM_011512087.2:c.-438-195A>G	XP_011510389.1:n.-438-195A>G
XM_024453197.1:c.-1292-195A>G	XP_024308965.1:n.-1292-195A>G
XM_024453198.1:c.-446-195A>G	XP_024308966.1:n.-446-195A>G
XM_024453199.1:c.-589-195A>G	XP_024308967.1:n.-589-195A>G
XM_024453201.1:c.-101+426A>G	XP_024308969.1:n.-101+426A>G
NM_001393486.1:c.-337-195A>G	NP_001380415.1:n.-337-195A>G
NM_001393488.1:c.-967-195A>G	NP_001380417.1:n.-967-195A>G
NM_001393489.1:c.-438-195A>G	NP_001380418.1:n.-438-195A>G
NM_003853.4:c.-337-195A>G	NP_003844.1:n.-337-195A>G