Canonical Allele Identifier: CA2480880288

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465212G= , CM000663.2:g.154465212G=	GRCh38
NC_000001.10:g.154437688G= , CM000663.1:g.154437688G=	GRCh37
NC_000001.9:g.152704312G=	NCBI36
NG_012087.1:g.65020G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1239G= MANE Select	ENSP00000357470.3:p.Leu413=
ENST00000344086.8:c.*47G=	ENSP00000340589.4:n.*47G=
ENST00000368485.7:c.1239G=	ENSP00000357470.3:p.Leu413=
ENST00000502679.1:n.552G=
ENST00000507256.1:n.437G=
NM_000565.3:c.1239G=	NP_000556.1:p.Leu413=
NM_181359.2:c.*47G=	NP_852004.1:n.*47G=
XM_005245139.1:c.1003G=	XP_005245196.1:p.Gly335=
XM_005245140.1:c.*80G=	XP_005245197.1:n.*80G=
XM_006711298.1:c.1287G=	XP_006711361.1:p.Leu429=
XM_006711299.2:c.*47G=	XP_006711362.1:n.*47G=
XM_005245139.2:c.1003G=	XP_005245196.1:p.Gly335=
XM_005245140.3:c.*80G=	XP_005245197.1:n.*80G=
XM_006711298.2:c.1287G=	XP_006711361.1:p.Leu429=
XM_006711299.4:c.*47G=	XP_006711362.1:n.*47G=
XM_017001199.2:c.1386G=	XP_016856688.1:p.Leu462=
XM_017001200.2:c.1338G=	XP_016856689.1:p.Leu446=
XM_017001201.2:c.*80G=	XP_016856690.1:n.*80G=
NM_000565.4:c.1239G= MANE Select	NP_000556.1:p.Leu413=
NM_181359.3:c.*47G=	NP_852004.1:n.*47G=
NM_001382769.1:c.1338G=	NP_001369698.1:p.Leu446=
NM_001382770.1:c.1332G=	NP_001369699.1:p.Leu444=
NM_001382771.1:c.1287G=	NP_001369700.1:p.Leu429=
NM_001382772.1:c.1233G=	NP_001369701.1:p.Leu411=
NM_001382773.1:c.*47G=	NP_001369702.1:n.*47G=
NM_001382774.1:c.879G=	NP_001369703.1:p.Leu293=