Canonical Allele Identifier: CA2480875695

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154454226_154454228delinsGTC , CM000663.2:g.154454226_154454228delinsGTC	GRCh38
NC_000001.10:g.154426702_154426704delinsGTC , CM000663.1:g.154426702_154426704delinsGTC	GRCh37
NC_000001.9:g.152693326_152693328delinsGTC	NCBI36
NG_012087.1:g.54034_54036delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1067-262_1067-260delinsGTC MANE Select	ENSP00000357470.3:n.1067-262_1067-260delinsGTC
ENST00000344086.8:c.1066+4246_1066+4248delinsGTC	ENSP00000340589.4:n.1066+4246_1066+4248delinsGTC
ENST00000368485.7:c.1067-262_1067-260delinsGTC	ENSP00000357470.3:n.1067-262_1067-260delinsGTC
ENST00000502679.1:n.118_120delinsGTC
ENST00000507256.1:n.265-262_265-260delinsGTC
ENST00000515190.1:c.475-262_475-260delinsGTC
NM_000565.3:c.1067-262_1067-260delinsGTC	NP_000556.1:n.1067-262_1067-260delinsGTC
NM_181359.2:c.1066+4246_1066+4248delinsGTC	NP_852004.1:n.1066+4246_1066+4248delinsGTC
XM_005245139.1:c.924+4246_924+4248delinsGTC	XP_005245196.1:n.924+4246_924+4248delinsGTC
XM_005245140.1:c.925-262_925-260delinsGTC	XP_005245197.1:n.925-262_925-260delinsGTC
XM_006711298.1:c.1115-262_1115-260delinsGTC	XP_006711361.1:n.1115-262_1115-260delinsGTC
XM_006711299.2:c.1114+4246_1114+4248delinsGTC	XP_006711362.1:n.1114+4246_1114+4248delinsGTC
XM_005245139.2:c.924+4246_924+4248delinsGTC	XP_005245196.1:n.924+4246_924+4248delinsGTC
XM_005245140.3:c.925-262_925-260delinsGTC	XP_005245197.1:n.925-262_925-260delinsGTC
XM_006711298.2:c.1115-262_1115-260delinsGTC	XP_006711361.1:n.1115-262_1115-260delinsGTC
XM_006711299.4:c.1114+4246_1114+4248delinsGTC	XP_006711362.1:n.1114+4246_1114+4248delinsGTC
XM_017001199.2:c.1213+55_1213+57delinsGTC	XP_016856688.1:n.1213+55_1213+57delinsGTC
XM_017001200.2:c.1165+55_1165+57delinsGTC	XP_016856689.1:n.1165+55_1165+57delinsGTC
XM_017001201.2:c.1023+55_1023+57delinsGTC	XP_016856690.1:n.1023+55_1023+57delinsGTC
NM_000565.4:c.1067-262_1067-260delinsGTC MANE Select	NP_000556.1:n.1067-262_1067-260delinsGTC
NM_181359.3:c.1066+4246_1066+4248delinsGTC	NP_852004.1:n.1066+4246_1066+4248delinsGTC
NM_001382769.1:c.1165+55_1165+57delinsGTC	NP_001369698.1:n.1165+55_1165+57delinsGTC
NM_001382770.1:c.1160-262_1160-260delinsGTC	NP_001369699.1:n.1160-262_1160-260delinsGTC
NM_001382771.1:c.1115-262_1115-260delinsGTC	NP_001369700.1:n.1115-262_1115-260delinsGTC
NM_001382772.1:c.1061-262_1061-260delinsGTC	NP_001369701.1:n.1061-262_1061-260delinsGTC
NM_001382773.1:c.1114+4246_1114+4248delinsGTC	NP_001369702.1:n.1114+4246_1114+4248delinsGTC
NM_001382774.1:c.707-262_707-260delinsGTC	NP_001369703.1:n.707-262_707-260delinsGTC