Canonical Allele Identifier: CA1007937902

Gene: IL6R

Linked Data

• gnomAD v3: 1-154454470-ATT-A
• gnomAD v4: 1-154454470-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154454479_154454480del , CM000663.2:g.154454479_154454480del	GRCh38
NC_000001.10:g.154426955_154426956del , CM000663.1:g.154426955_154426956del	GRCh37
NC_000001.9:g.152693579_152693580del	NCBI36
NG_012087.1:g.54287_54288del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1067-9_1067-8del MANE Select	ENSP00000357470.3:n.1067-9_1067-8del
ENST00000344086.8:c.1066+4499_1066+4500del	ENSP00000340589.4:n.1066+4499_1066+4500del
ENST00000368485.7:c.1067-9_1067-8del	ENSP00000357470.3:n.1067-9_1067-8del
ENST00000502679.1:n.371_372del
ENST00000507256.1:n.265-9_265-8del
ENST00000515190.1:c.475-9_475-8del
NM_000565.3:c.1067-9_1067-8del	NP_000556.1:n.1067-9_1067-8del
NM_181359.2:c.1066+4499_1066+4500del	NP_852004.1:n.1066+4499_1066+4500del
XM_005245139.1:c.924+4499_924+4500del	XP_005245196.1:n.924+4499_924+4500del
XM_005245140.1:c.925-9_925-8del	XP_005245197.1:n.925-9_925-8del
XM_006711298.1:c.1115-9_1115-8del	XP_006711361.1:n.1115-9_1115-8del
XM_006711299.2:c.1114+4499_1114+4500del	XP_006711362.1:n.1114+4499_1114+4500del
XM_005245139.2:c.924+4499_924+4500del	XP_005245196.1:n.924+4499_924+4500del
XM_005245140.3:c.925-9_925-8del	XP_005245197.1:n.925-9_925-8del
XM_006711298.2:c.1115-9_1115-8del	XP_006711361.1:n.1115-9_1115-8del
XM_006711299.4:c.1114+4499_1114+4500del	XP_006711362.1:n.1114+4499_1114+4500del
XM_017001199.2:c.1214-9_1214-8del	XP_016856688.1:n.1214-9_1214-8del
XM_017001200.2:c.1166-9_1166-8del	XP_016856689.1:n.1166-9_1166-8del
XM_017001201.2:c.1024-9_1024-8del	XP_016856690.1:n.1024-9_1024-8del
NM_000565.4:c.1067-9_1067-8del MANE Select	NP_000556.1:n.1067-9_1067-8del
NM_181359.3:c.1066+4499_1066+4500del	NP_852004.1:n.1066+4499_1066+4500del
NM_001382769.1:c.1166-9_1166-8del	NP_001369698.1:n.1166-9_1166-8del
NM_001382770.1:c.1160-9_1160-8del	NP_001369699.1:n.1160-9_1160-8del
NM_001382771.1:c.1115-9_1115-8del	NP_001369700.1:n.1115-9_1115-8del
NM_001382772.1:c.1061-9_1061-8del	NP_001369701.1:n.1061-9_1061-8del
NM_001382773.1:c.1114+4499_1114+4500del	NP_001369702.1:n.1114+4499_1114+4500del
NM_001382774.1:c.707-9_707-8del	NP_001369703.1:n.707-9_707-8del