Canonical Allele Identifier: CA1139974639

Gene: IL20

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206867232G= , CM000663.2:g.206867232G=	GRCh38
NC_000001.10:g.207040577G= , CM000663.1:g.207040577G=	GRCh37
NC_000001.9:g.205107200G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367098.6:c.379-152G= MANE Select	ENSP00000356065.1:n.379-152G=
ENST00000367096.7:c.379-152G=	ENSP00000356063.3:n.379-152G=
ENST00000367098.5:c.379-152G=	ENSP00000356065.1:n.379-152G=
ENST00000391930.3:c.378+596G=	ENSP00000375796.2:n.378+596G=
NM_018724.3:c.379-152G=	NP_061194.2:n.379-152G=
XM_005273152.2:c.634-152G=	XP_005273209.1:n.634-152G=
XM_005273152.3:c.634-152G=	XP_005273209.1:n.634-152G=
NM_001385165.1:c.378+596G=	NP_001372094.1:n.378+596G=
NM_001385166.1:c.379-152G=	NP_001372095.1:n.379-152G=
NM_001385167.1:c.379-152G=	NP_001372096.1:n.379-152G=
NM_018724.4:c.379-152G= MANE Select	NP_061194.2:n.379-152G=