Canonical Allele Identifier: CA2648156598
Gene: IL6R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154454478_154454480del , CM000663.2:g.154454478_154454480del GRCh38
NC_000001.10:g.154426954_154426956del , CM000663.1:g.154426954_154426956del GRCh37
NC_000001.9:g.152693578_152693580del NCBI36
NG_012087.1:g.54286_54288del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.1067-10_1067-8del MANE Select ENSP00000357470.3:n.1067-10_1067-8del
ENST00000344086.8:c.1066+4498_1066+4500del ENSP00000340589.4:n.1066+4498_1066+4500del
ENST00000368485.7:c.1067-10_1067-8del ENSP00000357470.3:n.1067-10_1067-8del
ENST00000502679.1:n.370_372del
ENST00000507256.1:n.265-10_265-8del
ENST00000515190.1:c.475-10_475-8del
NM_000565.3:c.1067-10_1067-8del NP_000556.1:n.1067-10_1067-8del
NM_181359.2:c.1066+4498_1066+4500del NP_852004.1:n.1066+4498_1066+4500del
XM_005245139.1:c.924+4498_924+4500del XP_005245196.1:n.924+4498_924+4500del
XM_005245140.1:c.925-10_925-8del XP_005245197.1:n.925-10_925-8del
XM_006711298.1:c.1115-10_1115-8del XP_006711361.1:n.1115-10_1115-8del
XM_006711299.2:c.1114+4498_1114+4500del XP_006711362.1:n.1114+4498_1114+4500del
XM_005245139.2:c.924+4498_924+4500del XP_005245196.1:n.924+4498_924+4500del
XM_005245140.3:c.925-10_925-8del XP_005245197.1:n.925-10_925-8del
XM_006711298.2:c.1115-10_1115-8del XP_006711361.1:n.1115-10_1115-8del
XM_006711299.4:c.1114+4498_1114+4500del XP_006711362.1:n.1114+4498_1114+4500del
XM_017001199.2:c.1214-10_1214-8del XP_016856688.1:n.1214-10_1214-8del
XM_017001200.2:c.1166-10_1166-8del XP_016856689.1:n.1166-10_1166-8del
XM_017001201.2:c.1024-10_1024-8del XP_016856690.1:n.1024-10_1024-8del
NM_000565.4:c.1067-10_1067-8del MANE Select NP_000556.1:n.1067-10_1067-8del
NM_181359.3:c.1066+4498_1066+4500del NP_852004.1:n.1066+4498_1066+4500del
NM_001382769.1:c.1166-10_1166-8del NP_001369698.1:n.1166-10_1166-8del
NM_001382770.1:c.1160-10_1160-8del NP_001369699.1:n.1160-10_1160-8del
NM_001382771.1:c.1115-10_1115-8del NP_001369700.1:n.1115-10_1115-8del
NM_001382772.1:c.1061-10_1061-8del NP_001369701.1:n.1061-10_1061-8del
NM_001382773.1:c.1114+4498_1114+4500del NP_001369702.1:n.1114+4498_1114+4500del
NM_001382774.1:c.707-10_707-8del NP_001369703.1:n.707-10_707-8del