Canonical Allele Identifier: CA1143835640

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154448150C= , CM000663.2:g.154448150C=	GRCh38
NC_000001.10:g.154420626C= , CM000663.1:g.154420626C=	GRCh37
NC_000001.9:g.152687250C=	NCBI36
NG_012087.1:g.47958C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368485.8:c.975C= MANE Select	ENSP00000357470.3:p.Asn325=
ENST00000344086.8:c.975C=	ENSP00000340589.4:p.Asn325=
ENST00000368485.7:c.975C=	ENSP00000357470.3:p.Asn325=
ENST00000476006.5:c.791C=
ENST00000507256.1:n.173C=
ENST00000515190.1:c.383C=
NM_000565.3:c.975C=	NP_000556.1:p.Asn325=
NM_181359.2:c.975C=	NP_852004.1:p.Asn325=
XM_005245139.1:c.833C=	XP_005245196.1:p.Thr278=
XM_005245140.1:c.833C=	XP_005245197.1:p.Thr278=
XM_006711298.1:c.1023C=	XP_006711361.1:p.Asn341=
XM_006711299.2:c.1023C=	XP_006711362.1:p.Asn341=
XM_005245139.2:c.833C=	XP_005245196.1:p.Thr278=
XM_005245140.3:c.833C=	XP_005245197.1:p.Thr278=
XM_006711298.2:c.1023C=	XP_006711361.1:p.Asn341=
XM_006711299.4:c.1023C=	XP_006711362.1:p.Asn341=
XM_017001199.2:c.1023C=	XP_016856688.1:p.Asn341=
XM_017001200.2:c.975C=	XP_016856689.1:p.Asn325=
XM_017001201.2:c.833C=	XP_016856690.1:p.Thr278=
NM_000565.4:c.975C= MANE Select	NP_000556.1:p.Asn325=
NM_181359.3:c.975C=	NP_852004.1:p.Asn325=
NM_001382769.1:c.975C=	NP_001369698.1:p.Asn325=
NM_001382770.1:c.1068C=	NP_001369699.1:p.Asn356=
NM_001382771.1:c.1023C=	NP_001369700.1:p.Asn341=
NM_001382772.1:c.969C=	NP_001369701.1:p.Asn323=
NM_001382773.1:c.1023C=	NP_001369702.1:p.Asn341=
NM_001382774.1:c.615C=	NP_001369703.1:p.Asn205=