Canonical Allele Identifier: CA2480875681

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154454205C= , CM000663.2:g.154454205C=	GRCh38
NC_000001.10:g.154426681C= , CM000663.1:g.154426681C=	GRCh37
NC_000001.9:g.152693305C=	NCBI36
NG_012087.1:g.54013C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1067-283C= MANE Select	ENSP00000357470.3:n.1067-283C=
ENST00000344086.8:c.1066+4225C=	ENSP00000340589.4:n.1066+4225C=
ENST00000368485.7:c.1067-283C=	ENSP00000357470.3:n.1067-283C=
ENST00000502679.1:n.97C=
ENST00000507256.1:n.265-283C=
ENST00000515190.1:c.475-283C=
NM_000565.3:c.1067-283C=	NP_000556.1:n.1067-283C=
NM_181359.2:c.1066+4225C=	NP_852004.1:n.1066+4225C=
XM_005245139.1:c.924+4225C=	XP_005245196.1:n.924+4225C=
XM_005245140.1:c.925-283C=	XP_005245197.1:n.925-283C=
XM_006711298.1:c.1115-283C=	XP_006711361.1:n.1115-283C=
XM_006711299.2:c.1114+4225C=	XP_006711362.1:n.1114+4225C=
XM_005245139.2:c.924+4225C=	XP_005245196.1:n.924+4225C=
XM_005245140.3:c.925-283C=	XP_005245197.1:n.925-283C=
XM_006711298.2:c.1115-283C=	XP_006711361.1:n.1115-283C=
XM_006711299.4:c.1114+4225C=	XP_006711362.1:n.1114+4225C=
XM_017001199.2:c.1213+34C=	XP_016856688.1:n.1213+34C=
XM_017001200.2:c.1165+34C=	XP_016856689.1:n.1165+34C=
XM_017001201.2:c.1023+34C=	XP_016856690.1:n.1023+34C=
NM_000565.4:c.1067-283C= MANE Select	NP_000556.1:n.1067-283C=
NM_181359.3:c.1066+4225C=	NP_852004.1:n.1066+4225C=
NM_001382769.1:c.1165+34C=	NP_001369698.1:n.1165+34C=
NM_001382770.1:c.1160-283C=	NP_001369699.1:n.1160-283C=
NM_001382771.1:c.1115-283C=	NP_001369700.1:n.1115-283C=
NM_001382772.1:c.1061-283C=	NP_001369701.1:n.1061-283C=
NM_001382773.1:c.1114+4225C=	NP_001369702.1:n.1114+4225C=
NM_001382774.1:c.707-283C=	NP_001369703.1:n.707-283C=