Canonical Allele Identifier: CA1144117555

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465231C= , CM000663.2:g.154465231C=	GRCh38
NC_000001.10:g.154437707C= , CM000663.1:g.154437707C=	GRCh37
NC_000001.9:g.152704331C=	NCBI36
NG_012087.1:g.65039C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1258C= MANE Select	ENSP00000357470.3:p.Pro420=
ENST00000344086.8:c.*66C=	ENSP00000340589.4:n.*66C=
ENST00000368485.7:c.1258C=	ENSP00000357470.3:p.Pro420=
ENST00000502679.1:n.571C=
ENST00000507256.1:n.456C=
NM_000565.3:c.1258C=	NP_000556.1:p.Pro420=
NM_181359.2:c.*66C=	NP_852004.1:n.*66C=
XM_005245139.1:c.1022C=	XP_005245196.1:p.Thr341=
XM_005245140.1:c.*99C=	XP_005245197.1:n.*99C=
XM_006711298.1:c.1306C=	XP_006711361.1:p.Pro436=
XM_006711299.2:c.*66C=	XP_006711362.1:n.*66C=
XM_005245139.2:c.1022C=	XP_005245196.1:p.Thr341=
XM_005245140.3:c.*99C=	XP_005245197.1:n.*99C=
XM_006711298.2:c.1306C=	XP_006711361.1:p.Pro436=
XM_006711299.4:c.*66C=	XP_006711362.1:n.*66C=
XM_017001199.2:c.1405C=	XP_016856688.1:p.Pro469=
XM_017001200.2:c.1357C=	XP_016856689.1:p.Pro453=
XM_017001201.2:c.*99C=	XP_016856690.1:n.*99C=
NM_000565.4:c.1258C= MANE Select	NP_000556.1:p.Pro420=
NM_181359.3:c.*66C=	NP_852004.1:n.*66C=
NM_001382769.1:c.1357C=	NP_001369698.1:p.Pro453=
NM_001382770.1:c.1351C=	NP_001369699.1:p.Pro451=
NM_001382771.1:c.1306C=	NP_001369700.1:p.Pro436=
NM_001382772.1:c.1252C=	NP_001369701.1:p.Pro418=
NM_001382773.1:c.*66C=	NP_001369702.1:n.*66C=
NM_001382774.1:c.898C=	NP_001369703.1:p.Pro300=