Canonical Allele Identifier: CA2480880464

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465689G= , CM000663.2:g.154465689G=	GRCh38
NC_000001.10:g.154438165G= , CM000663.1:g.154438165G=	GRCh37
NC_000001.9:g.152704789G=	NCBI36
NG_012087.1:g.65497G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*309G= MANE Select	ENSP00000357470.3:n.*309G=
ENST00000344086.8:c.*524G=	ENSP00000340589.4:n.*524G=
ENST00000368485.7:c.*309G=	ENSP00000357470.3:n.*309G=
NM_000565.3:c.*309G=	NP_000556.1:n.*309G=
NM_181359.2:c.*524G=	NP_852004.1:n.*524G=
XM_005245139.1:c.*397G=	XP_005245196.1:n.*397G=
XM_005245140.1:c.*557G=	XP_005245197.1:n.*557G=
XM_006711298.1:c.*309G=	XP_006711361.1:n.*309G=
XM_005245139.2:c.*397G=	XP_005245196.1:n.*397G=
XM_005245140.3:c.*557G=	XP_005245197.1:n.*557G=
XM_006711298.2:c.*309G=	XP_006711361.1:n.*309G=
XM_017001199.2:c.*309G=	XP_016856688.1:n.*309G=
XM_017001200.2:c.*309G=	XP_016856689.1:n.*309G=
XM_017001201.2:c.*557G=	XP_016856690.1:n.*557G=
NM_000565.4:c.*309G= MANE Select	NP_000556.1:n.*309G=
NM_181359.3:c.*524G=	NP_852004.1:n.*524G=
NM_001382769.1:c.*309G=	NP_001369698.1:n.*309G=
NM_001382770.1:c.*309G=	NP_001369699.1:n.*309G=
NM_001382771.1:c.*309G=	NP_001369700.1:n.*309G=
NM_001382772.1:c.*309G=	NP_001369701.1:n.*309G=
NM_001382773.1:c.*524G=	NP_001369702.1:n.*524G=
NM_001382774.1:c.*309G=	NP_001369703.1:n.*309G=