Canonical Allele Identifier: CA1143782604

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465157G= , CM000663.2:g.154465157G=	GRCh38
NC_000001.10:g.154437633G= , CM000663.1:g.154437633G=	GRCh37
NC_000001.9:g.152704257G=	NCBI36
NG_012087.1:g.64965G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1184G= MANE Select	ENSP00000357470.3:p.Arg395=
ENST00000344086.8:c.1090G=	ENSP00000340589.4:p.Gly364=
ENST00000368485.7:c.1184G=	ENSP00000357470.3:p.Arg395=
ENST00000502679.1:n.497G=
ENST00000507256.1:n.382G=
NM_000565.3:c.1184G=	NP_000556.1:p.Arg395=
NM_181359.2:c.1090G=	NP_852004.1:p.Gly364=
XM_005245139.1:c.948G=	XP_005245196.1:p.Ala316=
XM_005245140.1:c.*25G=	XP_005245197.1:n.*25G=
XM_006711298.1:c.1232G=	XP_006711361.1:p.Arg411=
XM_006711299.2:c.1138G=	XP_006711362.1:p.Gly380=
XM_005245139.2:c.948G=	XP_005245196.1:p.Ala316=
XM_005245140.3:c.*25G=	XP_005245197.1:n.*25G=
XM_006711298.2:c.1232G=	XP_006711361.1:p.Arg411=
XM_006711299.4:c.1138G=	XP_006711362.1:p.Gly380=
XM_017001199.2:c.1331G=	XP_016856688.1:p.Arg444=
XM_017001200.2:c.1283G=	XP_016856689.1:p.Arg428=
XM_017001201.2:c.*25G=	XP_016856690.1:n.*25G=
NM_000565.4:c.1184G= MANE Select	NP_000556.1:p.Arg395=
NM_181359.3:c.1090G=	NP_852004.1:p.Gly364=
NM_001382769.1:c.1283G=	NP_001369698.1:p.Arg428=
NM_001382770.1:c.1277G=	NP_001369699.1:p.Arg426=
NM_001382771.1:c.1232G=	NP_001369700.1:p.Arg411=
NM_001382772.1:c.1178G=	NP_001369701.1:p.Arg393=
NM_001382773.1:c.1138G=	NP_001369702.1:p.Gly380=
NM_001382774.1:c.824G=	NP_001369703.1:p.Arg275=