Canonical Allele Identifier: CA2480880256

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465143G= , CM000663.2:g.154465143G=	GRCh38
NC_000001.10:g.154437619G= , CM000663.1:g.154437619G=	GRCh37
NC_000001.9:g.152704243G=	NCBI36
NG_012087.1:g.64951G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1170G= MANE Select	ENSP00000357470.3:p.Lys390=
ENST00000344086.8:c.1076G=	ENSP00000340589.4:p.Arg359=
ENST00000368485.7:c.1170G=	ENSP00000357470.3:p.Lys390=
ENST00000502679.1:n.483G=
ENST00000507256.1:n.368G=
NM_000565.3:c.1170G=	NP_000556.1:p.Lys390=
NM_181359.2:c.1076G=	NP_852004.1:p.Arg359=
XM_005245139.1:c.934G=	XP_005245196.1:p.Asp312=
XM_005245140.1:c.*11G=	XP_005245197.1:n.*11G=
XM_006711298.1:c.1218G=	XP_006711361.1:p.Lys406=
XM_006711299.2:c.1124G=	XP_006711362.1:p.Arg375=
XM_005245139.2:c.934G=	XP_005245196.1:p.Asp312=
XM_005245140.3:c.*11G=	XP_005245197.1:n.*11G=
XM_006711298.2:c.1218G=	XP_006711361.1:p.Lys406=
XM_006711299.4:c.1124G=	XP_006711362.1:p.Arg375=
XM_017001199.2:c.1317G=	XP_016856688.1:p.Lys439=
XM_017001200.2:c.1269G=	XP_016856689.1:p.Lys423=
XM_017001201.2:c.*11G=	XP_016856690.1:n.*11G=
NM_000565.4:c.1170G= MANE Select	NP_000556.1:p.Lys390=
NM_181359.3:c.1076G=	NP_852004.1:p.Arg359=
NM_001382769.1:c.1269G=	NP_001369698.1:p.Lys423=
NM_001382770.1:c.1263G=	NP_001369699.1:p.Lys421=
NM_001382771.1:c.1218G=	NP_001369700.1:p.Lys406=
NM_001382772.1:c.1164G=	NP_001369701.1:p.Lys388=
NM_001382773.1:c.1124G=	NP_001369702.1:p.Arg375=
NM_001382774.1:c.810G=	NP_001369703.1:p.Lys270=