Canonical Allele Identifier: CA2746186225

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465662_154465663insGG , CM000663.2:g.154465662_154465663insGG	GRCh38
NC_000001.10:g.154438138_154438139insGG , CM000663.1:g.154438138_154438139insGG	GRCh37
NC_000001.9:g.152704762_152704763insGG	NCBI36
NG_012087.1:g.65470_65471insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*282_*283insGG MANE Select	ENSP00000357470.3:n.*282_*283insGG
ENST00000344086.8:c.*497_*498insGG	ENSP00000340589.4:n.*497_*498insGG
ENST00000368485.7:c.*282_*283insGG	ENSP00000357470.3:n.*282_*283insGG
NM_000565.3:c.*282_*283insGG	NP_000556.1:n.*282_*283insGG
NM_181359.2:c.*497_*498insGG	NP_852004.1:n.*497_*498insGG
XM_005245139.1:c.*370_*371insGG	XP_005245196.1:n.*370_*371insGG
XM_005245140.1:c.*530_*531insGG	XP_005245197.1:n.*530_*531insGG
XM_006711298.1:c.*282_*283insGG	XP_006711361.1:n.*282_*283insGG
XM_005245139.2:c.*370_*371insGG	XP_005245196.1:n.*370_*371insGG
XM_005245140.3:c.*530_*531insGG	XP_005245197.1:n.*530_*531insGG
XM_006711298.2:c.*282_*283insGG	XP_006711361.1:n.*282_*283insGG
XM_017001199.2:c.*282_*283insGG	XP_016856688.1:n.*282_*283insGG
XM_017001200.2:c.*282_*283insGG	XP_016856689.1:n.*282_*283insGG
XM_017001201.2:c.*530_*531insGG	XP_016856690.1:n.*530_*531insGG
NM_000565.4:c.*282_*283insGG MANE Select	NP_000556.1:n.*282_*283insGG
NM_181359.3:c.*497_*498insGG	NP_852004.1:n.*497_*498insGG
NM_001382769.1:c.*282_*283insGG	NP_001369698.1:n.*282_*283insGG
NM_001382770.1:c.*282_*283insGG	NP_001369699.1:n.*282_*283insGG
NM_001382771.1:c.*282_*283insGG	NP_001369700.1:n.*282_*283insGG
NM_001382772.1:c.*282_*283insGG	NP_001369701.1:n.*282_*283insGG
NM_001382773.1:c.*497_*498insGG	NP_001369702.1:n.*497_*498insGG
NM_001382774.1:c.*282_*283insGG	NP_001369703.1:n.*282_*283insGG