Canonical Allele Identifier: CA2480873195

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154448171G= , CM000663.2:g.154448171G=	GRCh38
NC_000001.10:g.154420647G= , CM000663.1:g.154420647G=	GRCh37
NC_000001.9:g.152687271G=	NCBI36
NG_012087.1:g.47979G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.996G= MANE Select	ENSP00000357470.3:p.Gln332=
ENST00000344086.8:c.996G=	ENSP00000340589.4:p.Gln332=
ENST00000368485.7:c.996G=	ENSP00000357470.3:p.Gln332=
ENST00000476006.5:c.812G=
ENST00000507256.1:n.194G=
ENST00000515190.1:c.404G=
NM_000565.3:c.996G=	NP_000556.1:p.Gln332=
NM_181359.2:c.996G=	NP_852004.1:p.Gln332=
XM_005245139.1:c.854G=	XP_005245196.1:p.Arg285=
XM_005245140.1:c.854G=	XP_005245197.1:p.Arg285=
XM_006711298.1:c.1044G=	XP_006711361.1:p.Gln348=
XM_006711299.2:c.1044G=	XP_006711362.1:p.Gln348=
XM_005245139.2:c.854G=	XP_005245196.1:p.Arg285=
XM_005245140.3:c.854G=	XP_005245197.1:p.Arg285=
XM_006711298.2:c.1044G=	XP_006711361.1:p.Gln348=
XM_006711299.4:c.1044G=	XP_006711362.1:p.Gln348=
XM_017001199.2:c.1044G=	XP_016856688.1:p.Gln348=
XM_017001200.2:c.996G=	XP_016856689.1:p.Gln332=
XM_017001201.2:c.854G=	XP_016856690.1:p.Arg285=
NM_000565.4:c.996G= MANE Select	NP_000556.1:p.Gln332=
NM_181359.3:c.996G=	NP_852004.1:p.Gln332=
NM_001382769.1:c.996G=	NP_001369698.1:p.Gln332=
NM_001382770.1:c.1089G=	NP_001369699.1:p.Gln363=
NM_001382771.1:c.1044G=	NP_001369700.1:p.Gln348=
NM_001382772.1:c.990G=	NP_001369701.1:p.Gln330=
NM_001382773.1:c.1044G=	NP_001369702.1:p.Gln348=
NM_001382774.1:c.636G=	NP_001369703.1:p.Gln212=