Canonical Allele Identifier: CA2480880257

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465145C= , CM000663.2:g.154465145C=	GRCh38
NC_000001.10:g.154437621C= , CM000663.1:g.154437621C=	GRCh37
NC_000001.9:g.152704245C=	NCBI36
NG_012087.1:g.64953C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1172C= MANE Select	ENSP00000357470.3:p.Thr391=
ENST00000344086.8:c.1078C=	ENSP00000340589.4:p.Arg360=
ENST00000368485.7:c.1172C=	ENSP00000357470.3:p.Thr391=
ENST00000502679.1:n.485C=
ENST00000507256.1:n.370C=
NM_000565.3:c.1172C=	NP_000556.1:p.Thr391=
NM_181359.2:c.1078C=	NP_852004.1:p.Arg360=
XM_005245139.1:c.936C=	XP_005245196.1:p.Asp312=
XM_005245140.1:c.*13C=	XP_005245197.1:n.*13C=
XM_006711298.1:c.1220C=	XP_006711361.1:p.Thr407=
XM_006711299.2:c.1126C=	XP_006711362.1:p.Arg376=
XM_005245139.2:c.936C=	XP_005245196.1:p.Asp312=
XM_005245140.3:c.*13C=	XP_005245197.1:n.*13C=
XM_006711298.2:c.1220C=	XP_006711361.1:p.Thr407=
XM_006711299.4:c.1126C=	XP_006711362.1:p.Arg376=
XM_017001199.2:c.1319C=	XP_016856688.1:p.Thr440=
XM_017001200.2:c.1271C=	XP_016856689.1:p.Thr424=
XM_017001201.2:c.*13C=	XP_016856690.1:n.*13C=
NM_000565.4:c.1172C= MANE Select	NP_000556.1:p.Thr391=
NM_181359.3:c.1078C=	NP_852004.1:p.Arg360=
NM_001382769.1:c.1271C=	NP_001369698.1:p.Thr424=
NM_001382770.1:c.1265C=	NP_001369699.1:p.Thr422=
NM_001382771.1:c.1220C=	NP_001369700.1:p.Thr407=
NM_001382772.1:c.1166C=	NP_001369701.1:p.Thr389=
NM_001382773.1:c.1126C=	NP_001369702.1:p.Arg376=
NM_001382774.1:c.812C=	NP_001369703.1:p.Thr271=