Canonical Allele Identifier: CA2480880455

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465658A= , CM000663.2:g.154465658A=	GRCh38
NC_000001.10:g.154438134A= , CM000663.1:g.154438134A=	GRCh37
NC_000001.9:g.152704758A=	NCBI36
NG_012087.1:g.65466A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*278A= MANE Select	ENSP00000357470.3:n.*278A=
ENST00000344086.8:c.*493A=	ENSP00000340589.4:n.*493A=
ENST00000368485.7:c.*278A=	ENSP00000357470.3:n.*278A=
NM_000565.3:c.*278A=	NP_000556.1:n.*278A=
NM_181359.2:c.*493A=	NP_852004.1:n.*493A=
XM_005245139.1:c.*366A=	XP_005245196.1:n.*366A=
XM_005245140.1:c.*526A=	XP_005245197.1:n.*526A=
XM_006711298.1:c.*278A=	XP_006711361.1:n.*278A=
XM_005245139.2:c.*366A=	XP_005245196.1:n.*366A=
XM_005245140.3:c.*526A=	XP_005245197.1:n.*526A=
XM_006711298.2:c.*278A=	XP_006711361.1:n.*278A=
XM_017001199.2:c.*278A=	XP_016856688.1:n.*278A=
XM_017001200.2:c.*278A=	XP_016856689.1:n.*278A=
XM_017001201.2:c.*526A=	XP_016856690.1:n.*526A=
NM_000565.4:c.*278A= MANE Select	NP_000556.1:n.*278A=
NM_181359.3:c.*493A=	NP_852004.1:n.*493A=
NM_001382769.1:c.*278A=	NP_001369698.1:n.*278A=
NM_001382770.1:c.*278A=	NP_001369699.1:n.*278A=
NM_001382771.1:c.*278A=	NP_001369700.1:n.*278A=
NM_001382772.1:c.*278A=	NP_001369701.1:n.*278A=
NM_001382773.1:c.*493A=	NP_001369702.1:n.*493A=
NM_001382774.1:c.*278A=	NP_001369703.1:n.*278A=