Canonical Allele Identifier: CA13449340
Gene: IL18 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112164002G>A , CM000673.2:g.112164002G>A GRCh38
NC_000011.9:g.112034725G>A , CM000673.1:g.112034725G>A GRCh37
NC_000011.8:g.111539935G>A NCBI36
NG_028143.1:g.5116C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000280357.12:c.-105C>T MANE Select ENSP00000280357.7:n.-105C>T
ENST00000280357.11:c.-105C>T ENSP00000280357.7:n.-105C>T
ENST00000524595.5:c.-105C>T ENSP00000434561.1:n.-105C>T
ENST00000525987.5:n.320-6417G>A
ENST00000528832.1:c.-126C>T ENSP00000434161.1:n.-126C>T
ENST00000531744.5:c.315-6417G>A ENSP00000456957.1:n.315-6417G>A
ENST00000532699.1:c.315-6417G>A ENSP00000456434.1:n.315-6417G>A
ENST00000533858.5:n.95C>T
ENST00000534225.1:n.92C>T
NM_001243211.1:c.-105C>T NP_001230140.1:n.-105C>T
NM_001562.3:c.-105C>T NP_001553.1:n.-105C>T
XM_011542805.1:c.-126C>T XP_011541107.1:n.-126C>T
XM_011542806.1:c.-126C>T XP_011541108.1:n.-126C>T
XM_011542806.2:c.-126C>T XP_011541108.1:n.-126C>T
NM_001562.4:c.-105C>T MANE Select NP_001553.1:n.-105C>T
NM_001243211.2:c.-105C>T NP_001230140.1:n.-105C>T
NM_001386420.1:c.-126C>T NP_001373349.1:n.-126C>T
Search 100 bp 5'
Search 100 bp 3'