Canonical Allele Identifier: CA228571112

Gene: IL18

Linked Data

• dbSNP Id: rs552606124
• gnomAD v3: 11-112162743-G-T
• gnomAD v4: 11-112162743-G-T
• MyVariant Identifiers: chr11:g.112033466G>T (hg19) ; chr11:g.112162743G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112162743G>T , CM000673.2:g.112162743G>T	GRCh38
NC_000011.9:g.112033466G>T , CM000673.1:g.112033466G>T	GRCh37
NC_000011.8:g.111538676G>T	NCBI36
NG_028143.1:g.6375C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280357.12:c.-9+1163C>A MANE Select	ENSP00000280357.7:n.-9+1163C>A
ENST00000280357.11:c.-9+1163C>A	ENSP00000280357.7:n.-9+1163C>A
ENST00000524595.5:c.-9+1163C>A	ENSP00000434561.1:n.-9+1163C>A
ENST00000525987.5:n.320-7676G>T
ENST00000528832.1:c.-30+1163C>A	ENSP00000434161.1:n.-30+1163C>A
ENST00000531744.5:c.315-7676G>T	ENSP00000456957.1:n.315-7676G>T
ENST00000532699.1:c.315-7676G>T	ENSP00000456434.1:n.315-7676G>T
ENST00000533858.5:n.191+1163C>A
ENST00000534225.1:n.188+1163C>A
NM_001243211.1:c.-9+1163C>A	NP_001230140.1:n.-9+1163C>A
NM_001562.3:c.-9+1163C>A	NP_001553.1:n.-9+1163C>A
XM_011542805.1:c.-30+1163C>A	XP_011541107.1:n.-30+1163C>A
XM_011542806.1:c.-30+1163C>A	XP_011541108.1:n.-30+1163C>A
XM_011542806.2:c.-30+1163C>A	XP_011541108.1:n.-30+1163C>A
NM_001562.4:c.-9+1163C>A MANE Select	NP_001553.1:n.-9+1163C>A
NM_001243211.2:c.-9+1163C>A	NP_001230140.1:n.-9+1163C>A
NM_001386420.1:c.-30+1163C>A	NP_001373349.1:n.-30+1163C>A