Canonical Allele Identifier: CA1694106260

Gene: IL6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22731537C= , CM000669.2:g.22731537C=	GRCh38
NC_000007.13:g.22771156C= , CM000669.1:g.22771156C=	GRCh37
NC_000007.12:g.22737681C=	NCBI36
NG_011640.1:g.9391C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000600.5:c.603C= MANE Select	NP_000591.1:p.Phe201=
ENST00000258743.10:c.603C= MANE Select	ENSP00000258743.5:p.Phe201=
NM_000600.3:c.603C=	NP_000591.1:p.Phe201=
NM_000600.4:c.603C=	NP_000591.1:p.Phe201=
NM_001318095.1:c.375C=	NP_001305024.1:p.Phe125=
NM_001318095.2:c.375C=	NP_001305024.1:p.Phe125=
NM_001371096.1:c.534C=	NP_001358025.1:p.Phe178=
ENST00000258743.9:c.603C=	ENSP00000258743.5:p.Phe201=
ENST00000401630.7:c.534C=	ENSP00000384928.3:p.Phe178=
ENST00000404625.5:c.603C=	ENSP00000385675.1:p.Phe201=
ENST00000407492.5:c.375C=	ENSP00000385043.1:p.Phe125=
ENST00000485300.1:n.828C=
XM_011515390.1:c.603C=	XP_011513692.1:p.Phe201=
XM_011515390.2:c.603C=	XP_011513692.1:p.Phe201=
XM_011515391.1:c.375C=	XP_011513693.1:p.Phe125=