Canonical Allele Identifier: CA1140026185

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154446403C= , CM000663.2:g.154446403C=	GRCh38
NC_000001.10:g.154418879C= , CM000663.1:g.154418879C=	GRCh37
NC_000001.9:g.152685503C=	NCBI36
NG_012087.1:g.46211C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000565.4:c.950-1722C= MANE Select	NP_000556.1:n.950-1722C=
ENST00000368485.8:c.950-1722C= MANE Select	ENSP00000357470.3:n.950-1722C=
NM_000565.3:c.950-1722C=	NP_000556.1:n.950-1722C=
NM_001382769.1:c.950-1722C=	NP_001369698.1:n.950-1722C=
NM_001382770.1:c.1042+361C=	NP_001369699.1:n.1042+361C=
NM_001382771.1:c.997+1309C=	NP_001369700.1:n.997+1309C=
NM_001382772.1:c.944-1722C=	NP_001369701.1:n.944-1722C=
NM_001382773.1:c.997+1309C=	NP_001369702.1:n.997+1309C=
NM_001382774.1:c.590-1722C=	NP_001369703.1:n.590-1722C=
NM_181359.2:c.950-1722C=	NP_852004.1:n.950-1722C=
NM_181359.3:c.950-1722C=	NP_852004.1:n.950-1722C=
ENST00000344086.8:c.950-1722C=	ENSP00000340589.4:n.950-1722C=
ENST00000368485.7:c.950-1722C=	ENSP00000357470.3:n.950-1722C=
ENST00000476006.5:c.765+1309C=
ENST00000507256.1:n.148-1722C=
ENST00000515190.1:c.358-1722C=
XM_005245139.1:c.808-1722C=	XP_005245196.1:n.808-1722C=
XM_005245139.2:c.808-1722C=	XP_005245196.1:n.808-1722C=
XM_005245140.1:c.808-1722C=	XP_005245197.1:n.808-1722C=
XM_005245140.3:c.808-1722C=	XP_005245197.1:n.808-1722C=
XM_006711298.1:c.997+1309C=	XP_006711361.1:n.997+1309C=
XM_006711298.2:c.997+1309C=	XP_006711361.1:n.997+1309C=
XM_006711299.2:c.997+1309C=	XP_006711362.1:n.997+1309C=
XM_006711299.4:c.997+1309C=	XP_006711362.1:n.997+1309C=
XM_017001199.2:c.997+1309C=	XP_016856688.1:n.997+1309C=
XM_017001200.2:c.950-1722C=	XP_016856689.1:n.950-1722C=
XM_017001201.2:c.808-1722C=	XP_016856690.1:n.808-1722C=