Canonical Allele Identifier: CA2480880303

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465264C= , CM000663.2:g.154465264C=	GRCh38
NC_000001.10:g.154437740C= , CM000663.1:g.154437740C=	GRCh37
NC_000001.9:g.152704364C=	NCBI36
NG_012087.1:g.65072C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1291C= MANE Select	ENSP00000357470.3:p.Pro431=
ENST00000344086.8:c.*99C=	ENSP00000340589.4:n.*99C=
ENST00000368485.7:c.1291C=	ENSP00000357470.3:p.Pro431=
ENST00000507256.1:n.489C=
NM_000565.3:c.1291C=	NP_000556.1:p.Pro431=
NM_181359.2:c.*99C=	NP_852004.1:n.*99C=
XM_005245139.1:c.1055C=	XP_005245196.1:p.Thr352=
XM_005245140.1:c.*132C=	XP_005245197.1:n.*132C=
XM_006711298.1:c.1339C=	XP_006711361.1:p.Pro447=
XM_005245139.2:c.1055C=	XP_005245196.1:p.Thr352=
XM_005245140.3:c.*132C=	XP_005245197.1:n.*132C=
XM_006711298.2:c.1339C=	XP_006711361.1:p.Pro447=
XM_017001199.2:c.1438C=	XP_016856688.1:p.Pro480=
XM_017001200.2:c.1390C=	XP_016856689.1:p.Pro464=
XM_017001201.2:c.*132C=	XP_016856690.1:n.*132C=
NM_000565.4:c.1291C= MANE Select	NP_000556.1:p.Pro431=
NM_181359.3:c.*99C=	NP_852004.1:n.*99C=
NM_001382769.1:c.1390C=	NP_001369698.1:p.Pro464=
NM_001382770.1:c.1384C=	NP_001369699.1:p.Pro462=
NM_001382771.1:c.1339C=	NP_001369700.1:p.Pro447=
NM_001382772.1:c.1285C=	NP_001369701.1:p.Pro429=
NM_001382773.1:c.*99C=	NP_001369702.1:n.*99C=
NM_001382774.1:c.931C=	NP_001369703.1:p.Pro311=