Canonical Allele Identifier: CA1007934003
Gene: IL6R HGNC NCBI

Linked Data

dbSNP Id: rs1690389990

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154448353G>A , CM000663.2:g.154448353G>A GRCh38
NC_000001.10:g.154420829G>A , CM000663.1:g.154420829G>A GRCh37
NC_000001.9:g.152687453G>A NCBI36
NG_012087.1:g.48161G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368485.8:c.996+182G>A MANE Select ENSP00000357470.3:n.996+182G>A
ENST00000344086.8:c.996+182G>A ENSP00000340589.4:n.996+182G>A
ENST00000368485.7:c.996+182G>A ENSP00000357470.3:n.996+182G>A
ENST00000476006.5:c.812+182G>A
ENST00000507256.1:n.194+182G>A
ENST00000515190.1:c.404+182G>A
NM_000565.3:c.996+182G>A NP_000556.1:n.996+182G>A
NM_181359.2:c.996+182G>A NP_852004.1:n.996+182G>A
XM_005245139.1:c.854+182G>A XP_005245196.1:n.854+182G>A
XM_005245140.1:c.854+182G>A XP_005245197.1:n.854+182G>A
XM_006711298.1:c.1044+182G>A XP_006711361.1:n.1044+182G>A
XM_006711299.2:c.1044+182G>A XP_006711362.1:n.1044+182G>A
XM_005245139.2:c.854+182G>A XP_005245196.1:n.854+182G>A
XM_005245140.3:c.854+182G>A XP_005245197.1:n.854+182G>A
XM_006711298.2:c.1044+182G>A XP_006711361.1:n.1044+182G>A
XM_006711299.4:c.1044+182G>A XP_006711362.1:n.1044+182G>A
XM_017001199.2:c.1044+182G>A XP_016856688.1:n.1044+182G>A
XM_017001200.2:c.996+182G>A XP_016856689.1:n.996+182G>A
XM_017001201.2:c.854+182G>A XP_016856690.1:n.854+182G>A
NM_000565.4:c.996+182G>A MANE Select NP_000556.1:n.996+182G>A
NM_181359.3:c.996+182G>A NP_852004.1:n.996+182G>A
NM_001382769.1:c.996+182G>A NP_001369698.1:n.996+182G>A
NM_001382770.1:c.1089+182G>A NP_001369699.1:n.1089+182G>A
NM_001382771.1:c.1044+182G>A NP_001369700.1:n.1044+182G>A
NM_001382772.1:c.990+182G>A NP_001369701.1:n.990+182G>A
NM_001382773.1:c.1044+182G>A NP_001369702.1:n.1044+182G>A
NM_001382774.1:c.636+182G>A NP_001369703.1:n.636+182G>A