Canonical Allele Identifier: CA4185467

Gene: IL6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22731419A>T , CM000669.2:g.22731419A>T	GRCh38
NC_000007.13:g.22771038A>T , CM000669.1:g.22771038A>T	GRCh37
NC_000007.12:g.22737563A>T	NCBI36
NG_011640.1:g.9273A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000600.5:c.485A>T MANE Select	NP_000591.1:p.Asp162Val
ENST00000258743.10:c.485A>T MANE Select	ENSP00000258743.5:p.Asp162Val
NM_000600.3:c.485A>T	NP_000591.1:p.Asp162Val
NM_000600.4:c.485A>T	NP_000591.1:p.Asp162Val
NM_001318095.1:c.257A>T	NP_001305024.1:p.Asp86Val
NM_001318095.2:c.257A>T	NP_001305024.1:p.Asp86Val
NM_001371096.1:c.416A>T	NP_001358025.1:p.Asp139Val
ENST00000258743.9:c.485A>T	ENSP00000258743.5:p.Asp162Val
ENST00000401630.7:c.416A>T	ENSP00000384928.3:p.Asp139Val
ENST00000404625.5:c.485A>T	ENSP00000385675.1:p.Asp162Val
ENST00000407492.5:c.257A>T	ENSP00000385043.1:p.Asp86Val
ENST00000485300.1:n.710A>T
XM_011515390.1:c.485A>T	XP_011513692.1:p.Asp162Val
XM_011515390.2:c.485A>T	XP_011513692.1:p.Asp162Val
XM_011515391.1:c.257A>T	XP_011513693.1:p.Asp86Val