Canonical Allele Identifier: CA2480880338

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465339C= , CM000663.2:g.154465339C=	GRCh38
NC_000001.10:g.154437815C= , CM000663.1:g.154437815C=	GRCh37
NC_000001.9:g.152704439C=	NCBI36
NG_012087.1:g.65147C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1366C= MANE Select	ENSP00000357470.3:p.Pro456=
ENST00000344086.8:c.*174C=	ENSP00000340589.4:n.*174C=
ENST00000368485.7:c.1366C=	ENSP00000357470.3:p.Pro456=
NM_000565.3:c.1366C=	NP_000556.1:p.Pro456=
NM_181359.2:c.*174C=	NP_852004.1:n.*174C=
XM_005245139.1:c.*47C=	XP_005245196.1:n.*47C=
XM_005245140.1:c.*207C=	XP_005245197.1:n.*207C=
XM_006711298.1:c.1414C=	XP_006711361.1:p.Pro472=
XM_005245139.2:c.*47C=	XP_005245196.1:n.*47C=
XM_005245140.3:c.*207C=	XP_005245197.1:n.*207C=
XM_006711298.2:c.1414C=	XP_006711361.1:p.Pro472=
XM_017001199.2:c.1513C=	XP_016856688.1:p.Pro505=
XM_017001200.2:c.1465C=	XP_016856689.1:p.Pro489=
XM_017001201.2:c.*207C=	XP_016856690.1:n.*207C=
NM_000565.4:c.1366C= MANE Select	NP_000556.1:p.Pro456=
NM_181359.3:c.*174C=	NP_852004.1:n.*174C=
NM_001382769.1:c.1465C=	NP_001369698.1:p.Pro489=
NM_001382770.1:c.1459C=	NP_001369699.1:p.Pro487=
NM_001382771.1:c.1414C=	NP_001369700.1:p.Pro472=
NM_001382772.1:c.1360C=	NP_001369701.1:p.Pro454=
NM_001382773.1:c.*174C=	NP_001369702.1:n.*174C=
NM_001382774.1:c.1006C=	NP_001369703.1:p.Pro336=