Canonical Allele Identifier: CA155240269

Gene: IL6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22728600C>T , CM000669.2:g.22728600C>T	GRCh38
NC_000007.13:g.22768219C>T , CM000669.1:g.22768219C>T	GRCh37
NC_000007.12:g.22734744C>T	NCBI36
NG_011640.1:g.6454C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.1424C>T
ENST00000258743.10:c.211-93C>T MANE Select	ENSP00000258743.5:n.211-93C>T
ENST00000258743.9:c.211-93C>T	ENSP00000258743.5:n.211-93C>T
ENST00000401630.7:c.142-93C>T	ENSP00000384928.3:n.142-93C>T
ENST00000401651.5:c.-18-93C>T	ENSP00000385718.1:n.-18-93C>T
ENST00000404625.5:c.211-93C>T	ENSP00000385675.1:n.211-93C>T
ENST00000406575.1:c.211-93C>T	ENSP00000385227.1:n.211-93C>T
ENST00000407492.5:c.-18-93C>T	ENSP00000385043.1:n.-18-93C>T
ENST00000426291.5:c.211-93C>T	ENSP00000405150.1:n.211-93C>T
ENST00000464710.1:n.101C>T
ENST00000485300.1:n.436-93C>T
NM_000600.3:c.211-93C>T	NP_000591.1:n.211-93C>T
XM_005249745.3:c.373-93C>T	XP_005249802.1:n.373-93C>T
XM_011515390.1:c.211-93C>T	XP_011513692.1:n.211-93C>T
XM_011515391.1:c.-18-93C>T	XP_011513693.1:n.-18-93C>T
NM_000600.4:c.211-93C>T	NP_000591.1:n.211-93C>T
NM_001318095.1:c.-18-93C>T	NP_001305024.1:n.-18-93C>T
XM_005249745.5:c.373-93C>T	XP_005249802.1:n.373-93C>T
XM_011515390.2:c.211-93C>T	XP_011513692.1:n.211-93C>T
NM_000600.5:c.211-93C>T MANE Select	NP_000591.1:n.211-93C>T
NM_001318095.2:c.-18-93C>T	NP_001305024.1:n.-18-93C>T
NM_001371096.1:c.142-93C>T	NP_001358025.1:n.142-93C>T