Canonical Allele Identifier: CA2480875821

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154454561C= , CM000663.2:g.154454561C=	GRCh38
NC_000001.10:g.154427037C= , CM000663.1:g.154427037C=	GRCh37
NC_000001.9:g.152693661C=	NCBI36
NG_012087.1:g.54369C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1140C= MANE Select	ENSP00000357470.3:p.Leu380=
ENST00000344086.8:c.1066+4581C=	ENSP00000340589.4:n.1066+4581C=
ENST00000368485.7:c.1140C=	ENSP00000357470.3:p.Leu380=
ENST00000502679.1:n.453C=
ENST00000507256.1:n.338C=
ENST00000515190.1:c.548C=
NM_000565.3:c.1140C=	NP_000556.1:p.Leu380=
NM_181359.2:c.1066+4581C=	NP_852004.1:n.1066+4581C=
XM_005245139.1:c.924+4581C=	XP_005245196.1:n.924+4581C=
XM_005245140.1:c.998C=	XP_005245197.1:p.Ser333=
XM_006711298.1:c.1188C=	XP_006711361.1:p.Leu396=
XM_006711299.2:c.1114+4581C=	XP_006711362.1:n.1114+4581C=
XM_005245139.2:c.924+4581C=	XP_005245196.1:n.924+4581C=
XM_005245140.3:c.998C=	XP_005245197.1:p.Ser333=
XM_006711298.2:c.1188C=	XP_006711361.1:p.Leu396=
XM_006711299.4:c.1114+4581C=	XP_006711362.1:n.1114+4581C=
XM_017001199.2:c.1287C=	XP_016856688.1:p.Leu429=
XM_017001200.2:c.1239C=	XP_016856689.1:p.Leu413=
XM_017001201.2:c.1097C=	XP_016856690.1:p.Ser366=
NM_000565.4:c.1140C= MANE Select	NP_000556.1:p.Leu380=
NM_181359.3:c.1066+4581C=	NP_852004.1:n.1066+4581C=
NM_001382769.1:c.1239C=	NP_001369698.1:p.Leu413=
NM_001382770.1:c.1233C=	NP_001369699.1:p.Leu411=
NM_001382771.1:c.1188C=	NP_001369700.1:p.Leu396=
NM_001382772.1:c.1134C=	NP_001369701.1:p.Leu378=
NM_001382773.1:c.1114+4581C=	NP_001369702.1:n.1114+4581C=
NM_001382774.1:c.780C=	NP_001369703.1:p.Leu260=