Canonical Allele Identifier: CA2480875734

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154454348_154454349delinsAT , CM000663.2:g.154454348_154454349delinsAT	GRCh38
NC_000001.10:g.154426824_154426825delinsAT , CM000663.1:g.154426824_154426825delinsAT	GRCh37
NC_000001.9:g.152693448_152693449delinsAT	NCBI36
NG_012087.1:g.54156_54157delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1067-140_1067-139delinsAT MANE Select	ENSP00000357470.3:n.1067-140_1067-139delinsAT
ENST00000344086.8:c.1066+4368_1066+4369delinsAT	ENSP00000340589.4:n.1066+4368_1066+4369delinsAT
ENST00000368485.7:c.1067-140_1067-139delinsAT	ENSP00000357470.3:n.1067-140_1067-139delinsAT
ENST00000502679.1:n.240_241delinsAT
ENST00000507256.1:n.265-140_265-139delinsAT
ENST00000515190.1:c.475-140_475-139delinsAT
NM_000565.3:c.1067-140_1067-139delinsAT	NP_000556.1:n.1067-140_1067-139delinsAT
NM_181359.2:c.1066+4368_1066+4369delinsAT	NP_852004.1:n.1066+4368_1066+4369delinsAT
XM_005245139.1:c.924+4368_924+4369delinsAT	XP_005245196.1:n.924+4368_924+4369delinsAT
XM_005245140.1:c.925-140_925-139delinsAT	XP_005245197.1:n.925-140_925-139delinsAT
XM_006711298.1:c.1115-140_1115-139delinsAT	XP_006711361.1:n.1115-140_1115-139delinsAT
XM_006711299.2:c.1114+4368_1114+4369delinsAT	XP_006711362.1:n.1114+4368_1114+4369delinsAT
XM_005245139.2:c.924+4368_924+4369delinsAT	XP_005245196.1:n.924+4368_924+4369delinsAT
XM_005245140.3:c.925-140_925-139delinsAT	XP_005245197.1:n.925-140_925-139delinsAT
XM_006711298.2:c.1115-140_1115-139delinsAT	XP_006711361.1:n.1115-140_1115-139delinsAT
XM_006711299.4:c.1114+4368_1114+4369delinsAT	XP_006711362.1:n.1114+4368_1114+4369delinsAT
XM_017001199.2:c.1214-140_1214-139delinsAT	XP_016856688.1:n.1214-140_1214-139delinsAT
XM_017001200.2:c.1166-140_1166-139delinsAT	XP_016856689.1:n.1166-140_1166-139delinsAT
XM_017001201.2:c.1024-140_1024-139delinsAT	XP_016856690.1:n.1024-140_1024-139delinsAT
NM_000565.4:c.1067-140_1067-139delinsAT MANE Select	NP_000556.1:n.1067-140_1067-139delinsAT
NM_181359.3:c.1066+4368_1066+4369delinsAT	NP_852004.1:n.1066+4368_1066+4369delinsAT
NM_001382769.1:c.1166-140_1166-139delinsAT	NP_001369698.1:n.1166-140_1166-139delinsAT
NM_001382770.1:c.1160-140_1160-139delinsAT	NP_001369699.1:n.1160-140_1160-139delinsAT
NM_001382771.1:c.1115-140_1115-139delinsAT	NP_001369700.1:n.1115-140_1115-139delinsAT
NM_001382772.1:c.1061-140_1061-139delinsAT	NP_001369701.1:n.1061-140_1061-139delinsAT
NM_001382773.1:c.1114+4368_1114+4369delinsAT	NP_001369702.1:n.1114+4368_1114+4369delinsAT
NM_001382774.1:c.707-140_707-139delinsAT	NP_001369703.1:n.707-140_707-139delinsAT