Canonical Allele Identifier: CA155240849

Gene: IL6

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22729088T>A , CM000669.2:g.22729088T>A	GRCh38
NC_000007.13:g.22768707T>A , CM000669.1:g.22768707T>A	GRCh37
NC_000007.12:g.22735232T>A	NCBI36
NG_011640.1:g.6942T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.1630+282T>A
ENST00000258743.10:c.324+282T>A MANE Select	ENSP00000258743.5:n.324+282T>A
ENST00000258743.9:c.324+282T>A	ENSP00000258743.5:n.324+282T>A
ENST00000401630.7:c.255+282T>A	ENSP00000384928.3:n.255+282T>A
ENST00000401651.5:c.96+282T>A	ENSP00000385718.1:n.96+282T>A
ENST00000404625.5:c.324+282T>A	ENSP00000385675.1:n.324+282T>A
ENST00000406575.1:c.324+282T>A	ENSP00000385227.1:n.324+282T>A
ENST00000407492.5:c.96+282T>A	ENSP00000385043.1:n.96+282T>A
ENST00000426291.5:c.324+282T>A	ENSP00000405150.1:n.324+282T>A
ENST00000464710.1:n.307+282T>A
ENST00000485300.1:n.549+282T>A
NM_000600.3:c.324+282T>A	NP_000591.1:n.324+282T>A
XM_005249745.3:c.486+282T>A	XP_005249802.1:n.486+282T>A
XM_011515390.1:c.324+282T>A	XP_011513692.1:n.324+282T>A
XM_011515391.1:c.96+282T>A	XP_011513693.1:n.96+282T>A
NM_000600.4:c.324+282T>A	NP_000591.1:n.324+282T>A
NM_001318095.1:c.96+282T>A	NP_001305024.1:n.96+282T>A
XM_005249745.5:c.486+282T>A	XP_005249802.1:n.486+282T>A
XM_011515390.2:c.324+282T>A	XP_011513692.1:n.324+282T>A
NM_000600.5:c.324+282T>A MANE Select	NP_000591.1:n.324+282T>A
NM_001318095.2:c.96+282T>A	NP_001305024.1:n.96+282T>A
NM_001371096.1:c.255+282T>A	NP_001358025.1:n.255+282T>A