Canonical Allele Identifier: CA2480880431

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465584T= , CM000663.2:g.154465584T=	GRCh38
NC_000001.10:g.154438060T= , CM000663.1:g.154438060T=	GRCh37
NC_000001.9:g.152704684T=	NCBI36
NG_012087.1:g.65392T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*204T= MANE Select	ENSP00000357470.3:n.*204T=
ENST00000344086.8:c.*419T=	ENSP00000340589.4:n.*419T=
ENST00000368485.7:c.*204T=	ENSP00000357470.3:n.*204T=
NM_000565.3:c.*204T=	NP_000556.1:n.*204T=
NM_181359.2:c.*419T=	NP_852004.1:n.*419T=
XM_005245139.1:c.*292T=	XP_005245196.1:n.*292T=
XM_005245140.1:c.*452T=	XP_005245197.1:n.*452T=
XM_006711298.1:c.*204T=	XP_006711361.1:n.*204T=
XM_005245139.2:c.*292T=	XP_005245196.1:n.*292T=
XM_005245140.3:c.*452T=	XP_005245197.1:n.*452T=
XM_006711298.2:c.*204T=	XP_006711361.1:n.*204T=
XM_017001199.2:c.*204T=	XP_016856688.1:n.*204T=
XM_017001200.2:c.*204T=	XP_016856689.1:n.*204T=
XM_017001201.2:c.*452T=	XP_016856690.1:n.*452T=
NM_000565.4:c.*204T= MANE Select	NP_000556.1:n.*204T=
NM_181359.3:c.*419T=	NP_852004.1:n.*419T=
NM_001382769.1:c.*204T=	NP_001369698.1:n.*204T=
NM_001382770.1:c.*204T=	NP_001369699.1:n.*204T=
NM_001382771.1:c.*204T=	NP_001369700.1:n.*204T=
NM_001382772.1:c.*204T=	NP_001369701.1:n.*204T=
NM_001382773.1:c.*419T=	NP_001369702.1:n.*419T=
NM_001382774.1:c.*204T=	NP_001369703.1:n.*204T=