Canonical Allele Identifier: CA2480880262

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465164G= , CM000663.2:g.154465164G=	GRCh38
NC_000001.10:g.154437640G= , CM000663.1:g.154437640G=	GRCh37
NC_000001.9:g.152704264G=	NCBI36
NG_012087.1:g.64972G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1191G= MANE Select	ENSP00000357470.3:p.Leu397=
ENST00000344086.8:c.1097G=	ENSP00000340589.4:p.Ter366=
ENST00000368485.7:c.1191G=	ENSP00000357470.3:p.Leu397=
ENST00000502679.1:n.504G=
ENST00000507256.1:n.389G=
NM_000565.3:c.1191G=	NP_000556.1:p.Leu397=
NM_181359.2:c.1097G=	NP_852004.1:p.Ter366=
XM_005245139.1:c.955G=	XP_005245196.1:p.Glu319=
XM_005245140.1:c.*32G=	XP_005245197.1:n.*32G=
XM_006711298.1:c.1239G=	XP_006711361.1:p.Leu413=
XM_006711299.2:c.1145G=	XP_006711362.1:p.Ter382=
XM_005245139.2:c.955G=	XP_005245196.1:p.Glu319=
XM_005245140.3:c.*32G=	XP_005245197.1:n.*32G=
XM_006711298.2:c.1239G=	XP_006711361.1:p.Leu413=
XM_006711299.4:c.1145G=	XP_006711362.1:p.Ter382=
XM_017001199.2:c.1338G=	XP_016856688.1:p.Leu446=
XM_017001200.2:c.1290G=	XP_016856689.1:p.Leu430=
XM_017001201.2:c.*32G=	XP_016856690.1:n.*32G=
NM_000565.4:c.1191G= MANE Select	NP_000556.1:p.Leu397=
NM_181359.3:c.1097G=	NP_852004.1:p.Ter366=
NM_001382769.1:c.1290G=	NP_001369698.1:p.Leu430=
NM_001382770.1:c.1284G=	NP_001369699.1:p.Leu428=
NM_001382771.1:c.1239G=	NP_001369700.1:p.Leu413=
NM_001382772.1:c.1185G=	NP_001369701.1:p.Leu395=
NM_001382773.1:c.1145G=	NP_001369702.1:p.Ter382=
NM_001382774.1:c.831G=	NP_001369703.1:p.Leu277=