Canonical Allele Identifier: CA2480880321

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465302G= , CM000663.2:g.154465302G=	GRCh38
NC_000001.10:g.154437778G= , CM000663.1:g.154437778G=	GRCh37
NC_000001.9:g.152704402G=	NCBI36
NG_012087.1:g.65110G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1329G= MANE Select	ENSP00000357470.3:p.Ser443=
ENST00000344086.8:c.*137G=	ENSP00000340589.4:n.*137G=
ENST00000368485.7:c.1329G=	ENSP00000357470.3:p.Ser443=
ENST00000507256.1:n.527G=
NM_000565.3:c.1329G=	NP_000556.1:p.Ser443=
NM_181359.2:c.*137G=	NP_852004.1:n.*137G=
XM_005245139.1:c.*10G=	XP_005245196.1:n.*10G=
XM_005245140.1:c.*170G=	XP_005245197.1:n.*170G=
XM_006711298.1:c.1377G=	XP_006711361.1:p.Ser459=
XM_005245139.2:c.*10G=	XP_005245196.1:n.*10G=
XM_005245140.3:c.*170G=	XP_005245197.1:n.*170G=
XM_006711298.2:c.1377G=	XP_006711361.1:p.Ser459=
XM_017001199.2:c.1476G=	XP_016856688.1:p.Ser492=
XM_017001200.2:c.1428G=	XP_016856689.1:p.Ser476=
XM_017001201.2:c.*170G=	XP_016856690.1:n.*170G=
NM_000565.4:c.1329G= MANE Select	NP_000556.1:p.Ser443=
NM_181359.3:c.*137G=	NP_852004.1:n.*137G=
NM_001382769.1:c.1428G=	NP_001369698.1:p.Ser476=
NM_001382770.1:c.1422G=	NP_001369699.1:p.Ser474=
NM_001382771.1:c.1377G=	NP_001369700.1:p.Ser459=
NM_001382772.1:c.1323G=	NP_001369701.1:p.Ser441=
NM_001382773.1:c.*137G=	NP_001369702.1:n.*137G=
NM_001382774.1:c.969G=	NP_001369703.1:p.Ser323=