Canonical Allele Identifier: CA2000578260

Gene: IL18

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112153104C= , CM000673.2:g.112153104C=	GRCh38
NC_000011.9:g.112023827C= , CM000673.1:g.112023827C=	GRCh37
NC_000011.8:g.111529037C=	NCBI36
NG_028143.1:g.16014G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001562.4:c.91+488G= MANE Select	NP_001553.1:n.91+488G=
ENST00000280357.12:c.91+488G= MANE Select	ENSP00000280357.7:n.91+488G=
NM_001243211.1:c.79+1871G=	NP_001230140.1:n.79+1871G=
NM_001243211.2:c.79+1871G=	NP_001230140.1:n.79+1871G=
NM_001386420.1:c.91+488G=	NP_001373349.1:n.91+488G=
NM_001562.3:c.91+488G=	NP_001553.1:n.91+488G=
ENST00000280357.11:c.91+488G=	ENSP00000280357.7:n.91+488G=
ENST00000524595.5:c.79+1871G=	ENSP00000434561.1:n.79+1871G=
ENST00000525987.5:n.320-17315C=
ENST00000528832.1:c.91+488G=	ENSP00000434161.1:n.91+488G=
ENST00000531744.5:c.315-17315C=	ENSP00000456957.1:n.315-17315C=
ENST00000532699.1:c.315-17315C=	ENSP00000456434.1:n.315-17315C=
ENST00000533858.5:n.278+1871G=
ENST00000534225.1:n.775G=
XM_011542805.1:c.79+1871G=	XP_011541107.1:n.79+1871G=
XM_011542806.1:c.91+488G=	XP_011541108.1:n.91+488G=
XM_011542806.2:c.91+488G=	XP_011541108.1:n.91+488G=