Canonical Allele Identifier: CA1007937907
Gene: IL6R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154454481_154454487del , CM000663.2:g.154454481_154454487del GRCh38
NC_000001.10:g.154426957_154426963del , CM000663.1:g.154426957_154426963del GRCh37
NC_000001.9:g.152693581_152693587del NCBI36
NG_012087.1:g.54289_54295del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.1067-7_1067-1del MANE Select ENSP00000357470.3:n.1067-7_1067-1del
ENST00000344086.8:c.1066+4501_1066+4507del ENSP00000340589.4:n.1066+4501_1066+4507del
ENST00000368485.7:c.1067-7_1067-1del ENSP00000357470.3:n.1067-7_1067-1del
ENST00000502679.1:n.373_379del
ENST00000507256.1:n.265-7_265-1del
ENST00000515190.1:c.475-7_475-1del
NM_000565.3:c.1067-7_1067-1del NP_000556.1:n.1067-7_1067-1del
NM_181359.2:c.1066+4501_1066+4507del NP_852004.1:n.1066+4501_1066+4507del
XM_005245139.1:c.924+4501_924+4507del XP_005245196.1:n.924+4501_924+4507del
XM_005245140.1:c.925-7_925-1del XP_005245197.1:n.925-7_925-1del
XM_006711298.1:c.1115-7_1115-1del XP_006711361.1:n.1115-7_1115-1del
XM_006711299.2:c.1114+4501_1114+4507del XP_006711362.1:n.1114+4501_1114+4507del
XM_005245139.2:c.924+4501_924+4507del XP_005245196.1:n.924+4501_924+4507del
XM_005245140.3:c.925-7_925-1del XP_005245197.1:n.925-7_925-1del
XM_006711298.2:c.1115-7_1115-1del XP_006711361.1:n.1115-7_1115-1del
XM_006711299.4:c.1114+4501_1114+4507del XP_006711362.1:n.1114+4501_1114+4507del
XM_017001199.2:c.1214-7_1214-1del XP_016856688.1:n.1214-7_1214-1del
XM_017001200.2:c.1166-7_1166-1del XP_016856689.1:n.1166-7_1166-1del
XM_017001201.2:c.1024-7_1024-1del XP_016856690.1:n.1024-7_1024-1del
NM_000565.4:c.1067-7_1067-1del MANE Select NP_000556.1:n.1067-7_1067-1del
NM_181359.3:c.1066+4501_1066+4507del NP_852004.1:n.1066+4501_1066+4507del
NM_001382769.1:c.1166-7_1166-1del NP_001369698.1:n.1166-7_1166-1del
NM_001382770.1:c.1160-7_1160-1del NP_001369699.1:n.1160-7_1160-1del
NM_001382771.1:c.1115-7_1115-1del NP_001369700.1:n.1115-7_1115-1del
NM_001382772.1:c.1061-7_1061-1del NP_001369701.1:n.1061-7_1061-1del
NM_001382773.1:c.1114+4501_1114+4507del NP_001369702.1:n.1114+4501_1114+4507del
NM_001382774.1:c.707-7_707-1del NP_001369703.1:n.707-7_707-1del