Canonical Allele Identifier: CA2480880283

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465204G= , CM000663.2:g.154465204G=	GRCh38
NC_000001.10:g.154437680G= , CM000663.1:g.154437680G=	GRCh37
NC_000001.9:g.152704304G=	NCBI36
NG_012087.1:g.65012G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1231G= MANE Select	ENSP00000357470.3:p.Gly411=
ENST00000344086.8:c.*39G=	ENSP00000340589.4:n.*39G=
ENST00000368485.7:c.1231G=	ENSP00000357470.3:p.Gly411=
ENST00000502679.1:n.544G=
ENST00000507256.1:n.429G=
NM_000565.3:c.1231G=	NP_000556.1:p.Gly411=
NM_181359.2:c.*39G=	NP_852004.1:n.*39G=
XM_005245139.1:c.995G=	XP_005245196.1:p.Gly332=
XM_005245140.1:c.*72G=	XP_005245197.1:n.*72G=
XM_006711298.1:c.1279G=	XP_006711361.1:p.Gly427=
XM_006711299.2:c.*39G=	XP_006711362.1:n.*39G=
XM_005245139.2:c.995G=	XP_005245196.1:p.Gly332=
XM_005245140.3:c.*72G=	XP_005245197.1:n.*72G=
XM_006711298.2:c.1279G=	XP_006711361.1:p.Gly427=
XM_006711299.4:c.*39G=	XP_006711362.1:n.*39G=
XM_017001199.2:c.1378G=	XP_016856688.1:p.Gly460=
XM_017001200.2:c.1330G=	XP_016856689.1:p.Gly444=
XM_017001201.2:c.*72G=	XP_016856690.1:n.*72G=
NM_000565.4:c.1231G= MANE Select	NP_000556.1:p.Gly411=
NM_181359.3:c.*39G=	NP_852004.1:n.*39G=
NM_001382769.1:c.1330G=	NP_001369698.1:p.Gly444=
NM_001382770.1:c.1324G=	NP_001369699.1:p.Gly442=
NM_001382771.1:c.1279G=	NP_001369700.1:p.Gly427=
NM_001382772.1:c.1225G=	NP_001369701.1:p.Gly409=
NM_001382773.1:c.*39G=	NP_001369702.1:n.*39G=
NM_001382774.1:c.871G=	NP_001369703.1:p.Gly291=