Canonical Allele Identifier: CA2580600774

Gene: IL18

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112152125A>C , CM000673.2:g.112152125A>C	GRCh38
NC_000011.9:g.112022848A>C , CM000673.1:g.112022848A>C	GRCh37
NC_000011.8:g.111528058A>C	NCBI36
NG_028143.1:g.16993T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001562.4:c.91+1467T>G MANE Select	NP_001553.1:n.91+1467T>G
ENST00000280357.12:c.91+1467T>G MANE Select	ENSP00000280357.7:n.91+1467T>G
NM_001243211.1:c.80-1919T>G	NP_001230140.1:n.80-1919T>G
NM_001243211.2:c.80-1919T>G	NP_001230140.1:n.80-1919T>G
NM_001386420.1:c.91+1467T>G	NP_001373349.1:n.91+1467T>G
NM_001562.3:c.91+1467T>G	NP_001553.1:n.91+1467T>G
ENST00000280357.11:c.91+1467T>G	ENSP00000280357.7:n.91+1467T>G
ENST00000524595.5:c.80-1919T>G	ENSP00000434561.1:n.80-1919T>G
ENST00000525987.5:n.320-18294A>C
ENST00000528832.1:c.91+1467T>G	ENSP00000434161.1:n.91+1467T>G
ENST00000531744.5:c.315-18294A>C	ENSP00000456957.1:n.315-18294A>C
ENST00000532699.1:c.315-18294A>C	ENSP00000456434.1:n.315-18294A>C
ENST00000533858.5:n.279-1053T>G
XM_011542805.1:c.80-1919T>G	XP_011541107.1:n.80-1919T>G
XM_011542806.1:c.91+1467T>G	XP_011541108.1:n.91+1467T>G
XM_011542806.2:c.91+1467T>G	XP_011541108.1:n.91+1467T>G