Canonical Allele Identifier: CA342628626
Gene: IL6R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154465285G>A , CM000663.2:g.154465285G>A GRCh38
NC_000001.10:g.154437761G>A , CM000663.1:g.154437761G>A GRCh37
NC_000001.9:g.152704385G>A NCBI36
NG_012087.1:g.65093G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.1312G>A MANE Select ENSP00000357470.3:p.Gly438Arg
ENST00000344086.8:c.*120G>A ENSP00000340589.4:n.*120G>A
ENST00000368485.7:c.1312G>A ENSP00000357470.3:p.Gly438Arg
ENST00000507256.1:n.510G>A
NM_000565.3:c.1312G>A NP_000556.1:p.Gly438Arg
NM_181359.2:c.*120G>A NP_852004.1:n.*120G>A
XM_005245139.1:c.1076G>A XP_005245196.1:p.Gly359Glu
XM_005245140.1:c.*153G>A XP_005245197.1:n.*153G>A
XM_006711298.1:c.1360G>A XP_006711361.1:p.Gly454Arg
XM_005245139.2:c.1076G>A XP_005245196.1:p.Gly359Glu
XM_005245140.3:c.*153G>A XP_005245197.1:n.*153G>A
XM_006711298.2:c.1360G>A XP_006711361.1:p.Gly454Arg
XM_017001199.2:c.1459G>A XP_016856688.1:p.Gly487Arg
XM_017001200.2:c.1411G>A XP_016856689.1:p.Gly471Arg
XM_017001201.2:c.*153G>A XP_016856690.1:n.*153G>A
NM_000565.4:c.1312G>A MANE Select NP_000556.1:p.Gly438Arg
NM_181359.3:c.*120G>A NP_852004.1:n.*120G>A
NM_001382769.1:c.1411G>A NP_001369698.1:p.Gly471Arg
NM_001382770.1:c.1405G>A NP_001369699.1:p.Gly469Arg
NM_001382771.1:c.1360G>A NP_001369700.1:p.Gly454Arg
NM_001382772.1:c.1306G>A NP_001369701.1:p.Gly436Arg
NM_001382773.1:c.*120G>A NP_001369702.1:n.*120G>A
NM_001382774.1:c.952G>A NP_001369703.1:p.Gly318Arg