Canonical Allele Identifier: CA1145050896
Gene: IL6R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154454278_154454300delinsAAACAAACAAACAAACAAACAAA , CM000663.2:g.154454278_154454300delinsAAACAAACAAACAAACAAACAAA GRCh38
NC_000001.10:g.154426754_154426776delinsAAACAAACAAACAAACAAACAAA , CM000663.1:g.154426754_154426776delinsAAACAAACAAACAAACAAACAAA GRCh37
NC_000001.9:g.152693378_152693400delinsAAACAAACAAACAAACAAACAAA NCBI36
NG_012087.1:g.54086_54108delinsAAACAAACAAACAAACAAACAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.1067-210_1067-188delinsAAACAAACAAACAAACAAACAAA MANE Select ENSP00000357470.3:n.1067-210_1067-188delinsAAACAAACAAACAAACAA...
ENST00000344086.8:c.1066+4298_1066+4320delinsAAACAAACAAACAAACAAACAAA ENSP00000340589.4:n.1066+4298_1066+4320delinsAAACAAACAAACAAAC...
ENST00000368485.7:c.1067-210_1067-188delinsAAACAAACAAACAAACAAACAAA ENSP00000357470.3:n.1067-210_1067-188delinsAAACAAACAAACAAACAA...
ENST00000502679.1:n.170_192delinsAAACAAACAAACAAACAAACAAA
ENST00000507256.1:n.265-210_265-188delinsAAACAAACAAACAAACAAACAAA
ENST00000515190.1:c.475-210_475-188delinsAAACAAACAAACAAACAAACAAA
NM_000565.3:c.1067-210_1067-188delinsAAACAAACAAACAAACAAACAAA NP_000556.1:n.1067-210_1067-188delinsAAACAAACAAACAAACAAACAAA
NM_181359.2:c.1066+4298_1066+4320delinsAAACAAACAAACAAACAAACAAA NP_852004.1:n.1066+4298_1066+4320delinsAAACAAACAAACAAACAAACAA...
XM_005245139.1:c.924+4298_924+4320delinsAAACAAACAAACAAACAAACAAA XP_005245196.1:n.924+4298_924+4320delinsAAACAAACAAACAAACAAACA...
XM_005245140.1:c.925-210_925-188delinsAAACAAACAAACAAACAAACAAA XP_005245197.1:n.925-210_925-188delinsAAACAAACAAACAAACAAACAAA...
XM_006711298.1:c.1115-210_1115-188delinsAAACAAACAAACAAACAAACAAA XP_006711361.1:n.1115-210_1115-188delinsAAACAAACAAACAAACAAACA...
XM_006711299.2:c.1114+4298_1114+4320delinsAAACAAACAAACAAACAAACAAA XP_006711362.1:n.1114+4298_1114+4320delinsAAACAAACAAACAAACAAA...
XM_005245139.2:c.924+4298_924+4320delinsAAACAAACAAACAAACAAACAAA XP_005245196.1:n.924+4298_924+4320delinsAAACAAACAAACAAACAAACA...
XM_005245140.3:c.925-210_925-188delinsAAACAAACAAACAAACAAACAAA XP_005245197.1:n.925-210_925-188delinsAAACAAACAAACAAACAAACAAA...
XM_006711298.2:c.1115-210_1115-188delinsAAACAAACAAACAAACAAACAAA XP_006711361.1:n.1115-210_1115-188delinsAAACAAACAAACAAACAAACA...
XM_006711299.4:c.1114+4298_1114+4320delinsAAACAAACAAACAAACAAACAAA XP_006711362.1:n.1114+4298_1114+4320delinsAAACAAACAAACAAACAAA...
XM_017001199.2:c.1213+107_1213+129delinsAAACAAACAAACAAACAAACAAA XP_016856688.1:n.1213+107_1213+129delinsAAACAAACAAACAAACAAACA...
XM_017001200.2:c.1165+107_1165+129delinsAAACAAACAAACAAACAAACAAA XP_016856689.1:n.1165+107_1165+129delinsAAACAAACAAACAAACAAACA...
XM_017001201.2:c.1023+107_1023+129delinsAAACAAACAAACAAACAAACAAA XP_016856690.1:n.1023+107_1023+129delinsAAACAAACAAACAAACAAACA...
NM_000565.4:c.1067-210_1067-188delinsAAACAAACAAACAAACAAACAAA MANE Select NP_000556.1:n.1067-210_1067-188delinsAAACAAACAAACAAACAAACAAA
NM_181359.3:c.1066+4298_1066+4320delinsAAACAAACAAACAAACAAACAAA NP_852004.1:n.1066+4298_1066+4320delinsAAACAAACAAACAAACAAACAA...
NM_001382769.1:c.1165+107_1165+129delinsAAACAAACAAACAAACAAACAAA NP_001369698.1:n.1165+107_1165+129delinsAAACAAACAAACAAACAAACA...
NM_001382770.1:c.1160-210_1160-188delinsAAACAAACAAACAAACAAACAAA NP_001369699.1:n.1160-210_1160-188delinsAAACAAACAAACAAACAAACA...
NM_001382771.1:c.1115-210_1115-188delinsAAACAAACAAACAAACAAACAAA NP_001369700.1:n.1115-210_1115-188delinsAAACAAACAAACAAACAAACA...
NM_001382772.1:c.1061-210_1061-188delinsAAACAAACAAACAAACAAACAAA NP_001369701.1:n.1061-210_1061-188delinsAAACAAACAAACAAACAAACA...
NM_001382773.1:c.1114+4298_1114+4320delinsAAACAAACAAACAAACAAACAAA NP_001369702.1:n.1114+4298_1114+4320delinsAAACAAACAAACAAACAAA...
NM_001382774.1:c.707-210_707-188delinsAAACAAACAAACAAACAAACAAA NP_001369703.1:n.707-210_707-188delinsAAACAAACAAACAAACAAACAAA...