Canonical Allele Identifier: CA1007944477
Gene: IL6R HGNC NCBI

Linked Data

dbSNP Id: rs1691520422

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154465629G>A , CM000663.2:g.154465629G>A GRCh38
NC_000001.10:g.154438105G>A , CM000663.1:g.154438105G>A GRCh37
NC_000001.9:g.152704729G>A NCBI36
NG_012087.1:g.65437G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.*249G>A MANE Select ENSP00000357470.3:n.*249G>A
ENST00000344086.8:c.*464G>A ENSP00000340589.4:n.*464G>A
ENST00000368485.7:c.*249G>A ENSP00000357470.3:n.*249G>A
NM_000565.3:c.*249G>A NP_000556.1:n.*249G>A
NM_181359.2:c.*464G>A NP_852004.1:n.*464G>A
XM_005245139.1:c.*337G>A XP_005245196.1:n.*337G>A
XM_005245140.1:c.*497G>A XP_005245197.1:n.*497G>A
XM_006711298.1:c.*249G>A XP_006711361.1:n.*249G>A
XM_005245139.2:c.*337G>A XP_005245196.1:n.*337G>A
XM_005245140.3:c.*497G>A XP_005245197.1:n.*497G>A
XM_006711298.2:c.*249G>A XP_006711361.1:n.*249G>A
XM_017001199.2:c.*249G>A XP_016856688.1:n.*249G>A
XM_017001200.2:c.*249G>A XP_016856689.1:n.*249G>A
XM_017001201.2:c.*497G>A XP_016856690.1:n.*497G>A
NM_000565.4:c.*249G>A MANE Select NP_000556.1:n.*249G>A
NM_181359.3:c.*464G>A NP_852004.1:n.*464G>A
NM_001382769.1:c.*249G>A NP_001369698.1:n.*249G>A
NM_001382770.1:c.*249G>A NP_001369699.1:n.*249G>A
NM_001382771.1:c.*249G>A NP_001369700.1:n.*249G>A
NM_001382772.1:c.*249G>A NP_001369701.1:n.*249G>A
NM_001382773.1:c.*464G>A NP_001369702.1:n.*464G>A
NM_001382774.1:c.*249G>A NP_001369703.1:n.*249G>A