Canonical Allele Identifier: CA2746186219

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465631_154465638del , CM000663.2:g.154465631_154465638del	GRCh38
NC_000001.10:g.154438107_154438114del , CM000663.1:g.154438107_154438114del	GRCh37
NC_000001.9:g.152704731_152704738del	NCBI36
NG_012087.1:g.65439_65446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*251_*258del MANE Select	ENSP00000357470.3:n.*251_*258del
ENST00000344086.8:c.*466_*473del	ENSP00000340589.4:n.*466_*473del
ENST00000368485.7:c.*251_*258del	ENSP00000357470.3:n.*251_*258del
NM_000565.3:c.*251_*258del	NP_000556.1:n.*251_*258del
NM_181359.2:c.*466_*473del	NP_852004.1:n.*466_*473del
XM_005245139.1:c.*339_*346del	XP_005245196.1:n.*339_*346del
XM_005245140.1:c.*499_*506del	XP_005245197.1:n.*499_*506del
XM_006711298.1:c.*251_*258del	XP_006711361.1:n.*251_*258del
XM_005245139.2:c.*339_*346del	XP_005245196.1:n.*339_*346del
XM_005245140.3:c.*499_*506del	XP_005245197.1:n.*499_*506del
XM_006711298.2:c.*251_*258del	XP_006711361.1:n.*251_*258del
XM_017001199.2:c.*251_*258del	XP_016856688.1:n.*251_*258del
XM_017001200.2:c.*251_*258del	XP_016856689.1:n.*251_*258del
XM_017001201.2:c.*499_*506del	XP_016856690.1:n.*499_*506del
NM_000565.4:c.*251_*258del MANE Select	NP_000556.1:n.*251_*258del
NM_181359.3:c.*466_*473del	NP_852004.1:n.*466_*473del
NM_001382769.1:c.*251_*258del	NP_001369698.1:n.*251_*258del
NM_001382770.1:c.*251_*258del	NP_001369699.1:n.*251_*258del
NM_001382771.1:c.*251_*258del	NP_001369700.1:n.*251_*258del
NM_001382772.1:c.*251_*258del	NP_001369701.1:n.*251_*258del
NM_001382773.1:c.*466_*473del	NP_001369702.1:n.*466_*473del
NM_001382774.1:c.*251_*258del	NP_001369703.1:n.*251_*258del