Canonical Allele Identifier: CA52930790
Gene: IL18RAP HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11465702

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102441432A>G , CM000664.2:g.102441432A>G GRCh38
NC_000002.11:g.103057892A>G , CM000664.1:g.103057892A>G GRCh37
NC_000002.10:g.102424324A>G NCBI36
NG_011481.1:g.27639A>G

Transcript Alleles

HGVS Amino-acid change
NM_003853.3:c.796+55A>G VV NP_003844.1:p.=
XM_011512087.1:c.370+55A>G XP_011510389.1:p.=
XM_011512088.1:c.370+55A>G XP_011510390.1:p.=
XM_011512089.1:c.796+55A>G XP_011510391.1:p.=
XR_923052.1:n.1133+55A>G
XM_011512087.2:c.370+55A>G XP_011510389.1:p.=
XM_011512088.2:c.370+55A>G XP_011510390.1:p.=
XM_024453197.1:c.796+55A>G XP_024308965.1:p.=
XM_024453198.1:c.796+55A>G XP_024308966.1:p.=
XM_024453199.1:c.796+55A>G XP_024308967.1:p.=
XM_024453200.1:c.796+55A>G XP_024308968.1:p.=
XM_024453201.1:c.796+55A>G XP_024308969.1:p.=
XR_001739011.2:n.1131+55A>G
ENST00000264260.6:c.796+55A>G ENSP00000264260.2:p.=
ENST00000409369.1:c.370+55A>G ENSP00000387201.1:p.=