Canonical Allele Identifier: CA2480875697

Gene: IL6R

Linked Data

• dbSNP Id: rs1690745991

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154454227_154454228insTTGCCTCAAG , CM000663.2:g.154454227_154454228insTTGCCTCAAG	GRCh38
NC_000001.10:g.154426703_154426704insTTGCCTCAAG , CM000663.1:g.154426703_154426704insTTGCCTCAAG	GRCh37
NC_000001.9:g.152693327_152693328insTTGCCTCAAG	NCBI36
NG_012087.1:g.54035_54036insTTGCCTCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1067-261_1067-260insTTGCCTCAAG MANE Select	ENSP00000357470.3:n.1067-261_1067-260insTTGCCTCAAG
ENST00000344086.8:c.1066+4247_1066+4248insTTGCCTCAAG	ENSP00000340589.4:n.1066+4247_1066+4248insTTGCCTCAAG
ENST00000368485.7:c.1067-261_1067-260insTTGCCTCAAG	ENSP00000357470.3:n.1067-261_1067-260insTTGCCTCAAG
ENST00000502679.1:n.119_120insTTGCCTCAAG
ENST00000507256.1:n.265-261_265-260insTTGCCTCAAG
ENST00000515190.1:c.475-261_475-260insTTGCCTCAAG
NM_000565.3:c.1067-261_1067-260insTTGCCTCAAG	NP_000556.1:n.1067-261_1067-260insTTGCCTCAAG
NM_181359.2:c.1066+4247_1066+4248insTTGCCTCAAG	NP_852004.1:n.1066+4247_1066+4248insTTGCCTCAAG
XM_005245139.1:c.924+4247_924+4248insTTGCCTCAAG	XP_005245196.1:n.924+4247_924+4248insTTGCCTCAAG
XM_005245140.1:c.925-261_925-260insTTGCCTCAAG	XP_005245197.1:n.925-261_925-260insTTGCCTCAAG
XM_006711298.1:c.1115-261_1115-260insTTGCCTCAAG	XP_006711361.1:n.1115-261_1115-260insTTGCCTCAAG
XM_006711299.2:c.1114+4247_1114+4248insTTGCCTCAAG	XP_006711362.1:n.1114+4247_1114+4248insTTGCCTCAAG
XM_005245139.2:c.924+4247_924+4248insTTGCCTCAAG	XP_005245196.1:n.924+4247_924+4248insTTGCCTCAAG
XM_005245140.3:c.925-261_925-260insTTGCCTCAAG	XP_005245197.1:n.925-261_925-260insTTGCCTCAAG
XM_006711298.2:c.1115-261_1115-260insTTGCCTCAAG	XP_006711361.1:n.1115-261_1115-260insTTGCCTCAAG
XM_006711299.4:c.1114+4247_1114+4248insTTGCCTCAAG	XP_006711362.1:n.1114+4247_1114+4248insTTGCCTCAAG
XM_017001199.2:c.1213+56_1213+57insTTGCCTCAAG	XP_016856688.1:n.1213+56_1213+57insTTGCCTCAAG
XM_017001200.2:c.1165+56_1165+57insTTGCCTCAAG	XP_016856689.1:n.1165+56_1165+57insTTGCCTCAAG
XM_017001201.2:c.1023+56_1023+57insTTGCCTCAAG	XP_016856690.1:n.1023+56_1023+57insTTGCCTCAAG
NM_000565.4:c.1067-261_1067-260insTTGCCTCAAG MANE Select	NP_000556.1:n.1067-261_1067-260insTTGCCTCAAG
NM_181359.3:c.1066+4247_1066+4248insTTGCCTCAAG	NP_852004.1:n.1066+4247_1066+4248insTTGCCTCAAG
NM_001382769.1:c.1165+56_1165+57insTTGCCTCAAG	NP_001369698.1:n.1165+56_1165+57insTTGCCTCAAG
NM_001382770.1:c.1160-261_1160-260insTTGCCTCAAG	NP_001369699.1:n.1160-261_1160-260insTTGCCTCAAG
NM_001382771.1:c.1115-261_1115-260insTTGCCTCAAG	NP_001369700.1:n.1115-261_1115-260insTTGCCTCAAG
NM_001382772.1:c.1061-261_1061-260insTTGCCTCAAG	NP_001369701.1:n.1061-261_1061-260insTTGCCTCAAG
NM_001382773.1:c.1114+4247_1114+4248insTTGCCTCAAG	NP_001369702.1:n.1114+4247_1114+4248insTTGCCTCAAG
NM_001382774.1:c.707-261_707-260insTTGCCTCAAG	NP_001369703.1:n.707-261_707-260insTTGCCTCAAG