Canonical Allele Identifier: CA1142409209

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465139A= , CM000663.2:g.154465139A=	GRCh38
NC_000001.10:g.154437615A= , CM000663.1:g.154437615A=	GRCh37
NC_000001.9:g.152704239A=	NCBI36
NG_012087.1:g.64947A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1166A= MANE Select	ENSP00000357470.3:p.Lys389=
ENST00000344086.8:c.1072A=	ENSP00000340589.4:p.Arg358=
ENST00000368485.7:c.1166A=	ENSP00000357470.3:p.Lys389=
ENST00000502679.1:n.479A=
ENST00000507256.1:n.364A=
NM_000565.3:c.1166A=	NP_000556.1:p.Lys389=
NM_181359.2:c.1072A=	NP_852004.1:p.Arg358=
XM_005245139.1:c.930A=	XP_005245196.1:p.Gln310=
XM_005245140.1:c.*7A=	XP_005245197.1:n.*7A=
XM_006711298.1:c.1214A=	XP_006711361.1:p.Lys405=
XM_006711299.2:c.1120A=	XP_006711362.1:p.Arg374=
XM_005245139.2:c.930A=	XP_005245196.1:p.Gln310=
XM_005245140.3:c.*7A=	XP_005245197.1:n.*7A=
XM_006711298.2:c.1214A=	XP_006711361.1:p.Lys405=
XM_006711299.4:c.1120A=	XP_006711362.1:p.Arg374=
XM_017001199.2:c.1313A=	XP_016856688.1:p.Lys438=
XM_017001200.2:c.1265A=	XP_016856689.1:p.Lys422=
XM_017001201.2:c.*7A=	XP_016856690.1:n.*7A=
NM_000565.4:c.1166A= MANE Select	NP_000556.1:p.Lys389=
NM_181359.3:c.1072A=	NP_852004.1:p.Arg358=
NM_001382769.1:c.1265A=	NP_001369698.1:p.Lys422=
NM_001382770.1:c.1259A=	NP_001369699.1:p.Lys420=
NM_001382771.1:c.1214A=	NP_001369700.1:p.Lys405=
NM_001382772.1:c.1160A=	NP_001369701.1:p.Lys387=
NM_001382773.1:c.1120A=	NP_001369702.1:p.Arg374=
NM_001382774.1:c.806A=	NP_001369703.1:p.Lys269=