Canonical Allele Identifier: CA2515709040

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154448281_154448282insGGCTCAT , CM000663.2:g.154448281_154448282insGGCTCAT	GRCh38
NC_000001.10:g.154420757_154420758insGGCTCAT , CM000663.1:g.154420757_154420758insGGCTCAT	GRCh37
NC_000001.9:g.152687381_152687382insGGCTCAT	NCBI36
NG_012087.1:g.48089_48090insGGCTCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000368485.8:c.996+110_996+111insGGCTCAT MANE Select	ENSP00000357470.3:n.996+110_996+111insGGC...
ENST00000344086.8:c.996+110_996+111insGGCTCAT	ENSP00000340589.4:n.996+110_996+111insGGC...
ENST00000368485.7:c.996+110_996+111insGGCTCAT	ENSP00000357470.3:n.996+110_996+111insGGC...
ENST00000476006.5:c.812+110_812+111insGGCTCAT
ENST00000507256.1:n.194+110_194+111insGGCTCAT
ENST00000515190.1:c.404+110_404+111insGGCTCAT
NM_000565.3:c.996+110_996+111insGGCTCAT	NP_000556.1:n.996+110_996+111insGGCTCAT
NM_181359.2:c.996+110_996+111insGGCTCAT	NP_852004.1:n.996+110_996+111insGGCTCAT
XM_005245139.1:c.854+110_854+111insGGCTCAT	XP_005245196.1:n.854+110_854+111insGGCTCA...
XM_005245140.1:c.854+110_854+111insGGCTCAT	XP_005245197.1:n.854+110_854+111insGGCTCA...
XM_006711298.1:c.1044+110_1044+111insGGCTCAT	XP_006711361.1:n.1044+110_1044+111insGGCT...
XM_006711299.2:c.1044+110_1044+111insGGCTCAT	XP_006711362.1:n.1044+110_1044+111insGGCT...
XM_005245139.2:c.854+110_854+111insGGCTCAT	XP_005245196.1:n.854+110_854+111insGGCTCA...
XM_005245140.3:c.854+110_854+111insGGCTCAT	XP_005245197.1:n.854+110_854+111insGGCTCA...
XM_006711298.2:c.1044+110_1044+111insGGCTCAT	XP_006711361.1:n.1044+110_1044+111insGGCT...
XM_006711299.4:c.1044+110_1044+111insGGCTCAT	XP_006711362.1:n.1044+110_1044+111insGGCT...
XM_017001199.2:c.1044+110_1044+111insGGCTCAT	XP_016856688.1:n.1044+110_1044+111insGGCT...
XM_017001200.2:c.996+110_996+111insGGCTCAT	XP_016856689.1:n.996+110_996+111insGGCTCA...
XM_017001201.2:c.854+110_854+111insGGCTCAT	XP_016856690.1:n.854+110_854+111insGGCTCA...
NM_000565.4:c.996+110_996+111insGGCTCAT MANE Select	NP_000556.1:n.996+110_996+111insGGCTCAT
NM_181359.3:c.996+110_996+111insGGCTCAT	NP_852004.1:n.996+110_996+111insGGCTCAT
NM_001382769.1:c.996+110_996+111insGGCTCAT	NP_001369698.1:n.996+110_996+111insGGCTCA...
NM_001382770.1:c.1089+110_1089+111insGGCTCAT	NP_001369699.1:n.1089+110_1089+111insGGCT...
NM_001382771.1:c.1044+110_1044+111insGGCTCAT	NP_001369700.1:n.1044+110_1044+111insGGCT...
NM_001382772.1:c.990+110_990+111insGGCTCAT	NP_001369701.1:n.990+110_990+111insGGCTCA...
NM_001382773.1:c.1044+110_1044+111insGGCTCAT	NP_001369702.1:n.1044+110_1044+111insGGCT...
NM_001382774.1:c.636+110_636+111insGGCTCAT	NP_001369703.1:n.636+110_636+111insGGCTCA...