Canonical Allele Identifier: CA2480872711

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154447354G= , CM000663.2:g.154447354G=	GRCh38
NC_000001.10:g.154419830G= , CM000663.1:g.154419830G=	GRCh37
NC_000001.9:g.152686454G=	NCBI36
NG_012087.1:g.47162G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368485.8:c.950-771G= MANE Select	ENSP00000357470.3:n.950-771G=
ENST00000344086.8:c.950-771G=	ENSP00000340589.4:n.950-771G=
ENST00000368485.7:c.950-771G=	ENSP00000357470.3:n.950-771G=
ENST00000476006.5:c.766-771G=
ENST00000507256.1:n.148-771G=
ENST00000515190.1:c.358-771G=
NM_000565.3:c.950-771G=	NP_000556.1:n.950-771G=
NM_181359.2:c.950-771G=	NP_852004.1:n.950-771G=
XM_005245139.1:c.808-771G=	XP_005245196.1:n.808-771G=
XM_005245140.1:c.808-771G=	XP_005245197.1:n.808-771G=
XM_006711298.1:c.998-771G=	XP_006711361.1:n.998-771G=
XM_006711299.2:c.998-771G=	XP_006711362.1:n.998-771G=
XM_005245139.2:c.808-771G=	XP_005245196.1:n.808-771G=
XM_005245140.3:c.808-771G=	XP_005245197.1:n.808-771G=
XM_006711298.2:c.998-771G=	XP_006711361.1:n.998-771G=
XM_006711299.4:c.998-771G=	XP_006711362.1:n.998-771G=
XM_017001199.2:c.998-771G=	XP_016856688.1:n.998-771G=
XM_017001200.2:c.950-771G=	XP_016856689.1:n.950-771G=
XM_017001201.2:c.808-771G=	XP_016856690.1:n.808-771G=
NM_000565.4:c.950-771G= MANE Select	NP_000556.1:n.950-771G=
NM_181359.3:c.950-771G=	NP_852004.1:n.950-771G=
NM_001382769.1:c.950-771G=	NP_001369698.1:n.950-771G=
NM_001382770.1:c.1043-771G=	NP_001369699.1:n.1043-771G=
NM_001382771.1:c.998-771G=	NP_001369700.1:n.998-771G=
NM_001382772.1:c.944-771G=	NP_001369701.1:n.944-771G=
NM_001382773.1:c.998-771G=	NP_001369702.1:n.998-771G=
NM_001382774.1:c.590-771G=	NP_001369703.1:n.590-771G=