Canonical Allele Identifier: CA2480880313

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465285G= , CM000663.2:g.154465285G=	GRCh38
NC_000001.10:g.154437761G= , CM000663.1:g.154437761G=	GRCh37
NC_000001.9:g.152704385G=	NCBI36
NG_012087.1:g.65093G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1312G= MANE Select	ENSP00000357470.3:p.Gly438=
ENST00000344086.8:c.*120G=	ENSP00000340589.4:n.*120G=
ENST00000368485.7:c.1312G=	ENSP00000357470.3:p.Gly438=
ENST00000507256.1:n.510G=
NM_000565.3:c.1312G=	NP_000556.1:p.Gly438=
NM_181359.2:c.*120G=	NP_852004.1:n.*120G=
XM_005245139.1:c.1076G=	XP_005245196.1:p.Gly359=
XM_005245140.1:c.*153G=	XP_005245197.1:n.*153G=
XM_006711298.1:c.1360G=	XP_006711361.1:p.Gly454=
XM_005245139.2:c.1076G=	XP_005245196.1:p.Gly359=
XM_005245140.3:c.*153G=	XP_005245197.1:n.*153G=
XM_006711298.2:c.1360G=	XP_006711361.1:p.Gly454=
XM_017001199.2:c.1459G=	XP_016856688.1:p.Gly487=
XM_017001200.2:c.1411G=	XP_016856689.1:p.Gly471=
XM_017001201.2:c.*153G=	XP_016856690.1:n.*153G=
NM_000565.4:c.1312G= MANE Select	NP_000556.1:p.Gly438=
NM_181359.3:c.*120G=	NP_852004.1:n.*120G=
NM_001382769.1:c.1411G=	NP_001369698.1:p.Gly471=
NM_001382770.1:c.1405G=	NP_001369699.1:p.Gly469=
NM_001382771.1:c.1360G=	NP_001369700.1:p.Gly454=
NM_001382772.1:c.1306G=	NP_001369701.1:p.Gly436=
NM_001382773.1:c.*120G=	NP_001369702.1:n.*120G=
NM_001382774.1:c.952G=	NP_001369703.1:p.Gly318=