Canonical Allele Identifier: CA2480880347

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465361A= , CM000663.2:g.154465361A=	GRCh38
NC_000001.10:g.154437837A= , CM000663.1:g.154437837A=	GRCh37
NC_000001.9:g.152704461A=	NCBI36
NG_012087.1:g.65169A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1388A= MANE Select	ENSP00000357470.3:p.Asp463=
ENST00000344086.8:c.*196A=	ENSP00000340589.4:n.*196A=
ENST00000368485.7:c.1388A=	ENSP00000357470.3:p.Asp463=
NM_000565.3:c.1388A=	NP_000556.1:p.Asp463=
NM_181359.2:c.*196A=	NP_852004.1:n.*196A=
XM_005245139.1:c.*69A=	XP_005245196.1:n.*69A=
XM_005245140.1:c.*229A=	XP_005245197.1:n.*229A=
XM_006711298.1:c.1436A=	XP_006711361.1:p.Asp479=
XM_005245139.2:c.*69A=	XP_005245196.1:n.*69A=
XM_005245140.3:c.*229A=	XP_005245197.1:n.*229A=
XM_006711298.2:c.1436A=	XP_006711361.1:p.Asp479=
XM_017001199.2:c.1535A=	XP_016856688.1:p.Asp512=
XM_017001200.2:c.1487A=	XP_016856689.1:p.Asp496=
XM_017001201.2:c.*229A=	XP_016856690.1:n.*229A=
NM_000565.4:c.1388A= MANE Select	NP_000556.1:p.Asp463=
NM_181359.3:c.*196A=	NP_852004.1:n.*196A=
NM_001382769.1:c.1487A=	NP_001369698.1:p.Asp496=
NM_001382770.1:c.1481A=	NP_001369699.1:p.Asp494=
NM_001382771.1:c.1436A=	NP_001369700.1:p.Asp479=
NM_001382772.1:c.1382A=	NP_001369701.1:p.Asp461=
NM_001382773.1:c.*196A=	NP_001369702.1:n.*196A=
NM_001382774.1:c.1028A=	NP_001369703.1:p.Asp343=