Canonical Allele Identifier: CA2480875750
Gene: IL6R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154454377_154454382delinsGTTCCT , CM000663.2:g.154454377_154454382delinsGTTCCT GRCh38
NC_000001.10:g.154426853_154426858delinsGTTCCT , CM000663.1:g.154426853_154426858delinsGTTCCT GRCh37
NC_000001.9:g.152693477_152693482delinsGTTCCT NCBI36
NG_012087.1:g.54185_54190delinsGTTCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.1067-111_1067-106delinsGTTCCT MANE Select ENSP00000357470.3:n.1067-111_1067-106delinsGTTCCT
ENST00000344086.8:c.1066+4397_1066+4402delinsGTTCCT ENSP00000340589.4:n.1066+4397_1066+4402delinsGTTCCT
ENST00000368485.7:c.1067-111_1067-106delinsGTTCCT ENSP00000357470.3:n.1067-111_1067-106delinsGTTCCT
ENST00000502679.1:n.269_274delinsGTTCCT
ENST00000507256.1:n.265-111_265-106delinsGTTCCT
ENST00000515190.1:c.475-111_475-106delinsGTTCCT
NM_000565.3:c.1067-111_1067-106delinsGTTCCT NP_000556.1:n.1067-111_1067-106delinsGTTCCT
NM_181359.2:c.1066+4397_1066+4402delinsGTTCCT NP_852004.1:n.1066+4397_1066+4402delinsGTTCCT
XM_005245139.1:c.924+4397_924+4402delinsGTTCCT XP_005245196.1:n.924+4397_924+4402delinsGTTCCT
XM_005245140.1:c.925-111_925-106delinsGTTCCT XP_005245197.1:n.925-111_925-106delinsGTTCCT
XM_006711298.1:c.1115-111_1115-106delinsGTTCCT XP_006711361.1:n.1115-111_1115-106delinsGTTCCT
XM_006711299.2:c.1114+4397_1114+4402delinsGTTCCT XP_006711362.1:n.1114+4397_1114+4402delinsGTTCCT
XM_005245139.2:c.924+4397_924+4402delinsGTTCCT XP_005245196.1:n.924+4397_924+4402delinsGTTCCT
XM_005245140.3:c.925-111_925-106delinsGTTCCT XP_005245197.1:n.925-111_925-106delinsGTTCCT
XM_006711298.2:c.1115-111_1115-106delinsGTTCCT XP_006711361.1:n.1115-111_1115-106delinsGTTCCT
XM_006711299.4:c.1114+4397_1114+4402delinsGTTCCT XP_006711362.1:n.1114+4397_1114+4402delinsGTTCCT
XM_017001199.2:c.1214-111_1214-106delinsGTTCCT XP_016856688.1:n.1214-111_1214-106delinsGTTCCT
XM_017001200.2:c.1166-111_1166-106delinsGTTCCT XP_016856689.1:n.1166-111_1166-106delinsGTTCCT
XM_017001201.2:c.1024-111_1024-106delinsGTTCCT XP_016856690.1:n.1024-111_1024-106delinsGTTCCT
NM_000565.4:c.1067-111_1067-106delinsGTTCCT MANE Select NP_000556.1:n.1067-111_1067-106delinsGTTCCT
NM_181359.3:c.1066+4397_1066+4402delinsGTTCCT NP_852004.1:n.1066+4397_1066+4402delinsGTTCCT
NM_001382769.1:c.1166-111_1166-106delinsGTTCCT NP_001369698.1:n.1166-111_1166-106delinsGTTCCT
NM_001382770.1:c.1160-111_1160-106delinsGTTCCT NP_001369699.1:n.1160-111_1160-106delinsGTTCCT
NM_001382771.1:c.1115-111_1115-106delinsGTTCCT NP_001369700.1:n.1115-111_1115-106delinsGTTCCT
NM_001382772.1:c.1061-111_1061-106delinsGTTCCT NP_001369701.1:n.1061-111_1061-106delinsGTTCCT
NM_001382773.1:c.1114+4397_1114+4402delinsGTTCCT NP_001369702.1:n.1114+4397_1114+4402delinsGTTCCT
NM_001382774.1:c.707-111_707-106delinsGTTCCT NP_001369703.1:n.707-111_707-106delinsGTTCCT