Canonical Allele Identifier: CA13492245
Gene: IL18 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112144038G>T , CM000673.2:g.112144038G>T GRCh38
NC_000011.9:g.112014761G>T , CM000673.1:g.112014761G>T GRCh37
NC_000011.8:g.111519971G>T NCBI36
NG_028143.1:g.25080C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000280357.12:c.361-221C>A MANE Select ENSP00000280357.7:n.361-221C>A
ENST00000280357.11:c.361-221C>A ENSP00000280357.7:n.361-221C>A
ENST00000524595.5:c.349-221C>A ENSP00000434561.1:n.349-221C>A
ENST00000525547.5:n.1137-221C>A
ENST00000525987.5:n.320-26381G>T
ENST00000528832.1:c.361-221C>A ENSP00000434161.1:n.361-221C>A
ENST00000531744.5:c.315-26381G>T ENSP00000456957.1:n.315-26381G>T
ENST00000532699.1:c.315-26381G>T ENSP00000456434.1:n.315-26381G>T
ENST00000533858.5:n.624-221C>A
NM_001243211.1:c.349-221C>A NP_001230140.1:n.349-221C>A
NM_001562.3:c.361-221C>A NP_001553.1:n.361-221C>A
XM_011542805.1:c.349-221C>A XP_011541107.1:n.349-221C>A
XM_011542806.1:c.361-221C>A XP_011541108.1:n.361-221C>A
XM_011542806.2:c.361-221C>A XP_011541108.1:n.361-221C>A
NM_001562.4:c.361-221C>A MANE Select NP_001553.1:n.361-221C>A
NM_001243211.2:c.349-221C>A NP_001230140.1:n.349-221C>A
NM_001386420.1:c.361-221C>A NP_001373349.1:n.361-221C>A
Search 100 bp 5'
Search 100 bp 3'