Canonical Allele Identifier: CA155239710

Gene: IL6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22728045C>G , CM000669.2:g.22728045C>G	GRCh38
NC_000007.13:g.22767664C>G , CM000669.1:g.22767664C>G	GRCh37
NC_000007.12:g.22734189C>G	NCBI36
NG_011640.1:g.5899C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.869C>G
ENST00000258743.10:c.210+411C>G MANE Select	ENSP00000258743.5:n.210+411C>G
ENST00000258743.9:c.210+411C>G	ENSP00000258743.5:n.210+411C>G
ENST00000401630.7:c.141+411C>G	ENSP00000384928.3:n.141+411C>G
ENST00000401651.5:c.-18-648C>G	ENSP00000385718.1:n.-18-648C>G
ENST00000404625.5:c.210+411C>G	ENSP00000385675.1:n.210+411C>G
ENST00000406575.1:c.210+411C>G	ENSP00000385227.1:n.210+411C>G
ENST00000407492.5:c.-18-648C>G	ENSP00000385043.1:n.-18-648C>G
ENST00000426291.5:c.210+411C>G	ENSP00000405150.1:n.210+411C>G
ENST00000485300.1:n.435+411C>G
NM_000600.3:c.210+411C>G	NP_000591.1:n.210+411C>G
XM_005249745.3:c.372+411C>G	XP_005249802.1:n.372+411C>G
XM_011515390.1:c.210+411C>G	XP_011513692.1:n.210+411C>G
XM_011515391.1:c.-18-648C>G	XP_011513693.1:n.-18-648C>G
NM_000600.4:c.210+411C>G	NP_000591.1:n.210+411C>G
NM_001318095.1:c.-18-648C>G	NP_001305024.1:n.-18-648C>G
XM_005249745.5:c.372+411C>G	XP_005249802.1:n.372+411C>G
XM_011515390.2:c.210+411C>G	XP_011513692.1:n.210+411C>G
NM_000600.5:c.210+411C>G MANE Select	NP_000591.1:n.210+411C>G
NM_001318095.2:c.-18-648C>G	NP_001305024.1:n.-18-648C>G
NM_001371096.1:c.141+411C>G	NP_001358025.1:n.141+411C>G