Canonical Allele Identifier: CA2480880381

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465450T= , CM000663.2:g.154465450T=	GRCh38
NC_000001.10:g.154437926T= , CM000663.1:g.154437926T=	GRCh37
NC_000001.9:g.152704550T=	NCBI36
NG_012087.1:g.65258T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*70T= MANE Select	ENSP00000357470.3:n.*70T=
ENST00000344086.8:c.*285T=	ENSP00000340589.4:n.*285T=
ENST00000368485.7:c.*70T=	ENSP00000357470.3:n.*70T=
NM_000565.3:c.*70T=	NP_000556.1:n.*70T=
NM_181359.2:c.*285T=	NP_852004.1:n.*285T=
XM_005245139.1:c.*158T=	XP_005245196.1:n.*158T=
XM_005245140.1:c.*318T=	XP_005245197.1:n.*318T=
XM_006711298.1:c.*70T=	XP_006711361.1:n.*70T=
XM_005245139.2:c.*158T=	XP_005245196.1:n.*158T=
XM_005245140.3:c.*318T=	XP_005245197.1:n.*318T=
XM_006711298.2:c.*70T=	XP_006711361.1:n.*70T=
XM_017001199.2:c.*70T=	XP_016856688.1:n.*70T=
XM_017001200.2:c.*70T=	XP_016856689.1:n.*70T=
XM_017001201.2:c.*318T=	XP_016856690.1:n.*318T=
NM_000565.4:c.*70T= MANE Select	NP_000556.1:n.*70T=
NM_181359.3:c.*285T=	NP_852004.1:n.*285T=
NM_001382769.1:c.*70T=	NP_001369698.1:n.*70T=
NM_001382770.1:c.*70T=	NP_001369699.1:n.*70T=
NM_001382771.1:c.*70T=	NP_001369700.1:n.*70T=
NM_001382772.1:c.*70T=	NP_001369701.1:n.*70T=
NM_001382773.1:c.*285T=	NP_001369702.1:n.*285T=
NM_001382774.1:c.*70T=	NP_001369703.1:n.*70T=