Canonical Allele Identifier: CA2480880274

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465186C= , CM000663.2:g.154465186C=	GRCh38
NC_000001.10:g.154437662C= , CM000663.1:g.154437662C=	GRCh37
NC_000001.9:g.152704286C=	NCBI36
NG_012087.1:g.64994C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1213C= MANE Select	ENSP00000357470.3:p.His405=
ENST00000344086.8:c.*21C=	ENSP00000340589.4:n.*21C=
ENST00000368485.7:c.1213C=	ENSP00000357470.3:p.His405=
ENST00000502679.1:n.526C=
ENST00000507256.1:n.411C=
NM_000565.3:c.1213C=	NP_000556.1:p.His405=
NM_181359.2:c.*21C=	NP_852004.1:n.*21C=
XM_005245139.1:c.977C=	XP_005245196.1:p.Ala326=
XM_005245140.1:c.*54C=	XP_005245197.1:n.*54C=
XM_006711298.1:c.1261C=	XP_006711361.1:p.His421=
XM_006711299.2:c.*21C=	XP_006711362.1:n.*21C=
XM_005245139.2:c.977C=	XP_005245196.1:p.Ala326=
XM_005245140.3:c.*54C=	XP_005245197.1:n.*54C=
XM_006711298.2:c.1261C=	XP_006711361.1:p.His421=
XM_006711299.4:c.*21C=	XP_006711362.1:n.*21C=
XM_017001199.2:c.1360C=	XP_016856688.1:p.His454=
XM_017001200.2:c.1312C=	XP_016856689.1:p.His438=
XM_017001201.2:c.*54C=	XP_016856690.1:n.*54C=
NM_000565.4:c.1213C= MANE Select	NP_000556.1:p.His405=
NM_181359.3:c.*21C=	NP_852004.1:n.*21C=
NM_001382769.1:c.1312C=	NP_001369698.1:p.His438=
NM_001382770.1:c.1306C=	NP_001369699.1:p.His436=
NM_001382771.1:c.1261C=	NP_001369700.1:p.His421=
NM_001382772.1:c.1207C=	NP_001369701.1:p.His403=
NM_001382773.1:c.*21C=	NP_001369702.1:n.*21C=
NM_001382774.1:c.853C=	NP_001369703.1:p.His285=