Canonical Allele Identifier: CA1694138941

Gene: IL6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22728505C= , CM000669.2:g.22728505C=	GRCh38
NC_000007.13:g.22768124C= , CM000669.1:g.22768124C=	GRCh37
NC_000007.12:g.22734649C=	NCBI36
NG_011640.1:g.6359C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000600.5:c.211-188C= MANE Select	NP_000591.1:n.211-188C=
ENST00000258743.10:c.211-188C= MANE Select	ENSP00000258743.5:n.211-188C=
NM_000600.3:c.211-188C=	NP_000591.1:n.211-188C=
NM_000600.4:c.211-188C=	NP_000591.1:n.211-188C=
NM_001318095.1:c.-18-188C=	NP_001305024.1:n.-18-188C=
NM_001318095.2:c.-18-188C=	NP_001305024.1:n.-18-188C=
NM_001371096.1:c.142-188C=	NP_001358025.1:n.142-188C=
ENST00000258743.9:c.211-188C=	ENSP00000258743.5:n.211-188C=
ENST00000401630.7:c.142-188C=	ENSP00000384928.3:n.142-188C=
ENST00000401651.5:c.-18-188C=	ENSP00000385718.1:n.-18-188C=
ENST00000404625.5:c.211-188C=	ENSP00000385675.1:n.211-188C=
ENST00000406575.1:c.211-188C=	ENSP00000385227.1:n.211-188C=
ENST00000407492.5:c.-18-188C=	ENSP00000385043.1:n.-18-188C=
ENST00000426291.5:c.211-188C=	ENSP00000405150.1:n.211-188C=
ENST00000464710.1:n.6C=
ENST00000464710.2:n.1329C=
ENST00000485300.1:n.436-188C=
XM_005249745.3:c.373-188C=	XP_005249802.1:n.373-188C=
XM_005249745.5:c.373-188C=	XP_005249802.1:n.373-188C=
XM_011515390.1:c.211-188C=	XP_011513692.1:n.211-188C=
XM_011515390.2:c.211-188C=	XP_011513692.1:n.211-188C=
XM_011515391.1:c.-18-188C=	XP_011513693.1:n.-18-188C=