Canonical Allele Identifier: CA52953233

Gene: IL18RAP

Linked Data

• dbSNP Id: rs949625435
• gnomAD v3: 2-102419354-T-G
• gnomAD v4: 2-102419354-T-G
• MyVariant Identifiers: chr2:g.103035814T>G (hg19) ; chr2:g.102419354T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419354T>G , CM000664.2:g.102419354T>G	GRCh38
NC_000002.11:g.103035814T>G , CM000664.1:g.103035814T>G	GRCh37
NC_000002.10:g.102402246T>G	NCBI36
NG_011481.1:g.5561T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264260.6:c.-337-207T>G	ENSP00000264260.2:n.-337-207T>G
NM_003853.3:c.-337-207T>G	NP_003844.1:n.-337-207T>G
XM_011512087.1:c.-438-207T>G	XP_011510389.1:n.-438-207T>G
XM_011512087.2:c.-438-207T>G	XP_011510389.1:n.-438-207T>G
XM_024453197.1:c.-1292-207T>G	XP_024308965.1:n.-1292-207T>G
XM_024453198.1:c.-446-207T>G	XP_024308966.1:n.-446-207T>G
XM_024453199.1:c.-589-207T>G	XP_024308967.1:n.-589-207T>G
XM_024453201.1:c.-101+414T>G	XP_024308969.1:n.-101+414T>G
NM_001393486.1:c.-337-207T>G	NP_001380415.1:n.-337-207T>G
NM_001393488.1:c.-967-207T>G	NP_001380417.1:n.-967-207T>G
NM_001393489.1:c.-438-207T>G	NP_001380418.1:n.-438-207T>G
NM_003853.4:c.-337-207T>G	NP_003844.1:n.-337-207T>G