Canonical Allele Identifier: CA2480880286

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465211T= , CM000663.2:g.154465211T=	GRCh38
NC_000001.10:g.154437687T= , CM000663.1:g.154437687T=	GRCh37
NC_000001.9:g.152704311T=	NCBI36
NG_012087.1:g.65019T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1238T= MANE Select	ENSP00000357470.3:p.Leu413=
ENST00000344086.8:c.*46T=	ENSP00000340589.4:n.*46T=
ENST00000368485.7:c.1238T=	ENSP00000357470.3:p.Leu413=
ENST00000502679.1:n.551T=
ENST00000507256.1:n.436T=
NM_000565.3:c.1238T=	NP_000556.1:p.Leu413=
NM_181359.2:c.*46T=	NP_852004.1:n.*46T=
XM_005245139.1:c.1002T=	XP_005245196.1:p.Ala334=
XM_005245140.1:c.*79T=	XP_005245197.1:n.*79T=
XM_006711298.1:c.1286T=	XP_006711361.1:p.Leu429=
XM_006711299.2:c.*46T=	XP_006711362.1:n.*46T=
XM_005245139.2:c.1002T=	XP_005245196.1:p.Ala334=
XM_005245140.3:c.*79T=	XP_005245197.1:n.*79T=
XM_006711298.2:c.1286T=	XP_006711361.1:p.Leu429=
XM_006711299.4:c.*46T=	XP_006711362.1:n.*46T=
XM_017001199.2:c.1385T=	XP_016856688.1:p.Leu462=
XM_017001200.2:c.1337T=	XP_016856689.1:p.Leu446=
XM_017001201.2:c.*79T=	XP_016856690.1:n.*79T=
NM_000565.4:c.1238T= MANE Select	NP_000556.1:p.Leu413=
NM_181359.3:c.*46T=	NP_852004.1:n.*46T=
NM_001382769.1:c.1337T=	NP_001369698.1:p.Leu446=
NM_001382770.1:c.1331T=	NP_001369699.1:p.Leu444=
NM_001382771.1:c.1286T=	NP_001369700.1:p.Leu429=
NM_001382772.1:c.1232T=	NP_001369701.1:p.Leu411=
NM_001382773.1:c.*46T=	NP_001369702.1:n.*46T=
NM_001382774.1:c.878T=	NP_001369703.1:p.Leu293=