Canonical Allele Identifier: CA2480873248
Gene: IL6R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154448335A= , CM000663.2:g.154448335A= GRCh38
NC_000001.10:g.154420811A= , CM000663.1:g.154420811A= GRCh37
NC_000001.9:g.152687435A= NCBI36
NG_012087.1:g.48143A=

Transcript Alleles

HGVS Amino-acid change
ENST00000368485.8:c.996+164A= MANE Select ENSP00000357470.3:n.996+164A=
ENST00000344086.8:c.996+164A= ENSP00000340589.4:n.996+164A=
ENST00000368485.7:c.996+164A= ENSP00000357470.3:n.996+164A=
ENST00000476006.5:c.812+164A=
ENST00000507256.1:n.194+164A=
ENST00000515190.1:c.404+164A=
NM_000565.3:c.996+164A= NP_000556.1:n.996+164A=
NM_181359.2:c.996+164A= NP_852004.1:n.996+164A=
XM_005245139.1:c.854+164A= XP_005245196.1:n.854+164A=
XM_005245140.1:c.854+164A= XP_005245197.1:n.854+164A=
XM_006711298.1:c.1044+164A= XP_006711361.1:n.1044+164A=
XM_006711299.2:c.1044+164A= XP_006711362.1:n.1044+164A=
XM_005245139.2:c.854+164A= XP_005245196.1:n.854+164A=
XM_005245140.3:c.854+164A= XP_005245197.1:n.854+164A=
XM_006711298.2:c.1044+164A= XP_006711361.1:n.1044+164A=
XM_006711299.4:c.1044+164A= XP_006711362.1:n.1044+164A=
XM_017001199.2:c.1044+164A= XP_016856688.1:n.1044+164A=
XM_017001200.2:c.996+164A= XP_016856689.1:n.996+164A=
XM_017001201.2:c.854+164A= XP_016856690.1:n.854+164A=
NM_000565.4:c.996+164A= MANE Select NP_000556.1:n.996+164A=
NM_181359.3:c.996+164A= NP_852004.1:n.996+164A=
NM_001382769.1:c.996+164A= NP_001369698.1:n.996+164A=
NM_001382770.1:c.1089+164A= NP_001369699.1:n.1089+164A=
NM_001382771.1:c.1044+164A= NP_001369700.1:n.1044+164A=
NM_001382772.1:c.990+164A= NP_001369701.1:n.990+164A=
NM_001382773.1:c.1044+164A= NP_001369702.1:n.1044+164A=
NM_001382774.1:c.636+164A= NP_001369703.1:n.636+164A=