Canonical Allele Identifier: CA1694138404

Gene: IL6 STEAP1B IL6-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22727417C= , CM000669.2:g.22727417C=	GRCh38
NC_000007.13:g.22767036C= , CM000669.1:g.22767036C=	GRCh37
NC_000007.12:g.22733561C=	NCBI36
NG_011640.1:g.5271C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.241C= (IL6)
ENST00000258743.10:c.20-27C= (IL6) MANE Select	ENSP00000258743.5:n.20-27C=
ENST00000650428.1:n.46+151G= (STEAP1B)
ENST00000258743.9:c.20-27C= (IL6)	ENSP00000258743.5:n.20-27C=
ENST00000401630.7:c.20-96C= (IL6)	ENSP00000384928.3:n.20-96C=
ENST00000401651.5:c.-19+136C= (IL6)	ENSP00000385718.1:n.-19+136C=
ENST00000404625.5:c.20-27C= (IL6)	ENSP00000385675.1:n.20-27C=
ENST00000406575.1:c.20-27C= (IL6)	ENSP00000385227.1:n.20-27C=
ENST00000407492.5:c.-19+136C= (IL6)	ENSP00000385043.1:n.-19+136C=
ENST00000426291.5:c.20-27C= (IL6)	ENSP00000405150.1:n.20-27C=
ENST00000485300.1:n.218C= (IL6)
NM_000600.3:c.20-27C= (IL6)	NP_000591.1:n.20-27C=
NR_131935.1:n.53+151G= (IL6-AS1)
XM_005249745.3:c.155C= (IL6)	XP_005249802.1:p.Pro52=
XM_011515390.1:c.20-27C= (IL6)	XP_011513692.1:n.20-27C=
XM_011515391.1:c.-19+136C= (IL6)	XP_011513693.1:n.-19+136C=
NM_000600.4:c.20-27C= (IL6)	NP_000591.1:n.20-27C=
NM_001318095.1:c.-19+136C= (IL6)	NP_001305024.1:n.-19+136C=
XM_005249745.5:c.155C= (IL6)	XP_005249802.1:p.Pro52=
XM_011515390.2:c.20-27C= (IL6)	XP_011513692.1:n.20-27C=
NM_000600.5:c.20-27C= (IL6) MANE Select	NP_000591.1:n.20-27C=
NM_001318095.2:c.-19+136C= (IL6)	NP_001305024.1:n.-19+136C=
NM_001371096.1:c.20-96C= (IL6)	NP_001358025.1:n.20-96C=