Canonical Allele Identifier: CA2480880443
Gene: IL6R HGNC NCBI

Linked Data

dbSNP Id: rs1691520984

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154465640del , CM000663.2:g.154465640del GRCh38
NC_000001.10:g.154438116del , CM000663.1:g.154438116del GRCh37
NC_000001.9:g.152704740del NCBI36
NG_012087.1:g.65448del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.*260del MANE Select ENSP00000357470.3:n.*260del
ENST00000344086.8:c.*475del ENSP00000340589.4:n.*475del
ENST00000368485.7:c.*260del ENSP00000357470.3:n.*260del
NM_000565.3:c.*260del NP_000556.1:n.*260del
NM_181359.2:c.*475del NP_852004.1:n.*475del
XM_005245139.1:c.*348del XP_005245196.1:n.*348del
XM_005245140.1:c.*508del XP_005245197.1:n.*508del
XM_006711298.1:c.*260del XP_006711361.1:n.*260del
XM_005245139.2:c.*348del XP_005245196.1:n.*348del
XM_005245140.3:c.*508del XP_005245197.1:n.*508del
XM_006711298.2:c.*260del XP_006711361.1:n.*260del
XM_017001199.2:c.*260del XP_016856688.1:n.*260del
XM_017001200.2:c.*260del XP_016856689.1:n.*260del
XM_017001201.2:c.*508del XP_016856690.1:n.*508del
NM_000565.4:c.*260del MANE Select NP_000556.1:n.*260del
NM_181359.3:c.*475del NP_852004.1:n.*475del
NM_001382769.1:c.*260del NP_001369698.1:n.*260del
NM_001382770.1:c.*260del NP_001369699.1:n.*260del
NM_001382771.1:c.*260del NP_001369700.1:n.*260del
NM_001382772.1:c.*260del NP_001369701.1:n.*260del
NM_001382773.1:c.*475del NP_001369702.1:n.*475del
NM_001382774.1:c.*260del NP_001369703.1:n.*260del