Canonical Allele Identifier: CA2746186220
Gene: IL6R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154465642_154465645del , CM000663.2:g.154465642_154465645del GRCh38
NC_000001.10:g.154438118_154438121del , CM000663.1:g.154438118_154438121del GRCh37
NC_000001.9:g.152704742_152704745del NCBI36
NG_012087.1:g.65450_65453del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.*262_*265del MANE Select ENSP00000357470.3:n.*262_*265del
ENST00000344086.8:c.*477_*480del ENSP00000340589.4:n.*477_*480del
ENST00000368485.7:c.*262_*265del ENSP00000357470.3:n.*262_*265del
NM_000565.3:c.*262_*265del NP_000556.1:n.*262_*265del
NM_181359.2:c.*477_*480del NP_852004.1:n.*477_*480del
XM_005245139.1:c.*350_*353del XP_005245196.1:n.*350_*353del
XM_005245140.1:c.*510_*513del XP_005245197.1:n.*510_*513del
XM_006711298.1:c.*262_*265del XP_006711361.1:n.*262_*265del
XM_005245139.2:c.*350_*353del XP_005245196.1:n.*350_*353del
XM_005245140.3:c.*510_*513del XP_005245197.1:n.*510_*513del
XM_006711298.2:c.*262_*265del XP_006711361.1:n.*262_*265del
XM_017001199.2:c.*262_*265del XP_016856688.1:n.*262_*265del
XM_017001200.2:c.*262_*265del XP_016856689.1:n.*262_*265del
XM_017001201.2:c.*510_*513del XP_016856690.1:n.*510_*513del
NM_000565.4:c.*262_*265del MANE Select NP_000556.1:n.*262_*265del
NM_181359.3:c.*477_*480del NP_852004.1:n.*477_*480del
NM_001382769.1:c.*262_*265del NP_001369698.1:n.*262_*265del
NM_001382770.1:c.*262_*265del NP_001369699.1:n.*262_*265del
NM_001382771.1:c.*262_*265del NP_001369700.1:n.*262_*265del
NM_001382772.1:c.*262_*265del NP_001369701.1:n.*262_*265del
NM_001382773.1:c.*477_*480del NP_001369702.1:n.*477_*480del
NM_001382774.1:c.*262_*265del NP_001369703.1:n.*262_*265del