Canonical Allele Identifier: CA366973719

Gene: IL6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22731420T>G , CM000669.2:g.22731420T>G	GRCh38
NC_000007.13:g.22771039T>G , CM000669.1:g.22771039T>G	GRCh37
NC_000007.12:g.22737564T>G	NCBI36
NG_011640.1:g.9274T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258743.10:c.486T>G MANE Select	ENSP00000258743.5:p.Asp162Glu
ENST00000258743.9:c.486T>G	ENSP00000258743.5:p.Asp162Glu
ENST00000401630.7:c.417T>G	ENSP00000384928.3:p.Asp139Glu
ENST00000404625.5:c.486T>G	ENSP00000385675.1:p.Asp162Glu
ENST00000407492.5:c.258T>G	ENSP00000385043.1:p.Asp86Glu
ENST00000485300.1:n.711T>G
NM_000600.3:c.486T>G	NP_000591.1:p.Asp162Glu
XM_011515390.1:c.486T>G	XP_011513692.1:p.Asp162Glu
XM_011515391.1:c.258T>G	XP_011513693.1:p.Asp86Glu
NM_000600.4:c.486T>G	NP_000591.1:p.Asp162Glu
NM_001318095.1:c.258T>G	NP_001305024.1:p.Asp86Glu
XM_011515390.2:c.486T>G	XP_011513692.1:p.Asp162Glu
NM_000600.5:c.486T>G MANE Select	NP_000591.1:p.Asp162Glu
NM_001318095.2:c.258T>G	NP_001305024.1:p.Asp86Glu
NM_001371096.1:c.417T>G	NP_001358025.1:p.Asp139Glu