Canonical Allele Identifier: CA2480873191

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154448153G= , CM000663.2:g.154448153G=	GRCh38
NC_000001.10:g.154420629G= , CM000663.1:g.154420629G=	GRCh37
NC_000001.9:g.152687253G=	NCBI36
NG_012087.1:g.47961G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368485.8:c.978G= MANE Select	ENSP00000357470.3:p.Glu326=
ENST00000344086.8:c.978G=	ENSP00000340589.4:p.Glu326=
ENST00000368485.7:c.978G=	ENSP00000357470.3:p.Glu326=
ENST00000476006.5:c.794G=
ENST00000507256.1:n.176G=
ENST00000515190.1:c.386G=
NM_000565.3:c.978G=	NP_000556.1:p.Glu326=
NM_181359.2:c.978G=	NP_852004.1:p.Glu326=
XM_005245139.1:c.836G=	XP_005245196.1:p.Arg279=
XM_005245140.1:c.836G=	XP_005245197.1:p.Arg279=
XM_006711298.1:c.1026G=	XP_006711361.1:p.Glu342=
XM_006711299.2:c.1026G=	XP_006711362.1:p.Glu342=
XM_005245139.2:c.836G=	XP_005245196.1:p.Arg279=
XM_005245140.3:c.836G=	XP_005245197.1:p.Arg279=
XM_006711298.2:c.1026G=	XP_006711361.1:p.Glu342=
XM_006711299.4:c.1026G=	XP_006711362.1:p.Glu342=
XM_017001199.2:c.1026G=	XP_016856688.1:p.Glu342=
XM_017001200.2:c.978G=	XP_016856689.1:p.Glu326=
XM_017001201.2:c.836G=	XP_016856690.1:p.Arg279=
NM_000565.4:c.978G= MANE Select	NP_000556.1:p.Glu326=
NM_181359.3:c.978G=	NP_852004.1:p.Glu326=
NM_001382769.1:c.978G=	NP_001369698.1:p.Glu326=
NM_001382770.1:c.1071G=	NP_001369699.1:p.Glu357=
NM_001382771.1:c.1026G=	NP_001369700.1:p.Glu342=
NM_001382772.1:c.972G=	NP_001369701.1:p.Glu324=
NM_001382773.1:c.1026G=	NP_001369702.1:p.Glu342=
NM_001382774.1:c.618G=	NP_001369703.1:p.Glu206=