Canonical Allele Identifier: CA754321698

Gene: IL18RAP

Linked Data

• dbSNP Id: rs1194167226
• MyVariant Identifiers: chr2:g.103035943C>T (hg19) ; chr2:g.102419483C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419483C>T , CM000664.2:g.102419483C>T	GRCh38
NC_000002.11:g.103035943C>T , CM000664.1:g.103035943C>T	GRCh37
NC_000002.10:g.102402375C>T	NCBI36
NG_011481.1:g.5690C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264260.6:c.-337-78C>T	ENSP00000264260.2:n.-337-78C>T
ENST00000450855.1:c.-415C>T	ENSP00000389815.1:n.-415C>T
NM_003853.3:c.-337-78C>T	NP_003844.1:n.-337-78C>T
XM_011512087.1:c.-438-78C>T	XP_011510389.1:n.-438-78C>T
XM_011512087.2:c.-438-78C>T	XP_011510389.1:n.-438-78C>T
XM_024453197.1:c.-1292-78C>T	XP_024308965.1:n.-1292-78C>T
XM_024453198.1:c.-446-78C>T	XP_024308966.1:n.-446-78C>T
XM_024453199.1:c.-589-78C>T	XP_024308967.1:n.-589-78C>T
XM_024453201.1:c.-101+543C>T	XP_024308969.1:n.-101+543C>T
NM_001393486.1:c.-337-78C>T	NP_001380415.1:n.-337-78C>T
NM_001393488.1:c.-967-78C>T	NP_001380417.1:n.-967-78C>T
NM_001393489.1:c.-438-78C>T	NP_001380418.1:n.-438-78C>T
NM_003853.4:c.-337-78C>T	NP_003844.1:n.-337-78C>T