Canonical Allele Identifier: CA2648156814
Gene: IL6R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154465444_154465446del , CM000663.2:g.154465444_154465446del GRCh38
NC_000001.10:g.154437920_154437922del , CM000663.1:g.154437920_154437922del GRCh37
NC_000001.9:g.152704544_152704546del NCBI36
NG_012087.1:g.65252_65254del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.*64_*66del MANE Select ENSP00000357470.3:n.*64_*66del
ENST00000344086.8:c.*279_*281del ENSP00000340589.4:n.*279_*281del
ENST00000368485.7:c.*64_*66del ENSP00000357470.3:n.*64_*66del
NM_000565.3:c.*64_*66del NP_000556.1:n.*64_*66del
NM_181359.2:c.*279_*281del NP_852004.1:n.*279_*281del
XM_005245139.1:c.*152_*154del XP_005245196.1:n.*152_*154del
XM_005245140.1:c.*312_*314del XP_005245197.1:n.*312_*314del
XM_006711298.1:c.*64_*66del XP_006711361.1:n.*64_*66del
XM_005245139.2:c.*152_*154del XP_005245196.1:n.*152_*154del
XM_005245140.3:c.*312_*314del XP_005245197.1:n.*312_*314del
XM_006711298.2:c.*64_*66del XP_006711361.1:n.*64_*66del
XM_017001199.2:c.*64_*66del XP_016856688.1:n.*64_*66del
XM_017001200.2:c.*64_*66del XP_016856689.1:n.*64_*66del
XM_017001201.2:c.*312_*314del XP_016856690.1:n.*312_*314del
NM_000565.4:c.*64_*66del MANE Select NP_000556.1:n.*64_*66del
NM_181359.3:c.*279_*281del NP_852004.1:n.*279_*281del
NM_001382769.1:c.*64_*66del NP_001369698.1:n.*64_*66del
NM_001382770.1:c.*64_*66del NP_001369699.1:n.*64_*66del
NM_001382771.1:c.*64_*66del NP_001369700.1:n.*64_*66del
NM_001382772.1:c.*64_*66del NP_001369701.1:n.*64_*66del
NM_001382773.1:c.*279_*281del NP_001369702.1:n.*279_*281del
NM_001382774.1:c.*64_*66del NP_001369703.1:n.*64_*66del