Canonical Allele Identifier: CA2480880322

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465304G= , CM000663.2:g.154465304G=	GRCh38
NC_000001.10:g.154437780G= , CM000663.1:g.154437780G=	GRCh37
NC_000001.9:g.152704404G=	NCBI36
NG_012087.1:g.65112G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1331G= MANE Select	ENSP00000357470.3:p.Ser444=
ENST00000344086.8:c.*139G=	ENSP00000340589.4:n.*139G=
ENST00000368485.7:c.1331G=	ENSP00000357470.3:p.Ser444=
ENST00000507256.1:n.529G=
NM_000565.3:c.1331G=	NP_000556.1:p.Ser444=
NM_181359.2:c.*139G=	NP_852004.1:n.*139G=
XM_005245139.1:c.*12G=	XP_005245196.1:n.*12G=
XM_005245140.1:c.*172G=	XP_005245197.1:n.*172G=
XM_006711298.1:c.1379G=	XP_006711361.1:p.Ser460=
XM_005245139.2:c.*12G=	XP_005245196.1:n.*12G=
XM_005245140.3:c.*172G=	XP_005245197.1:n.*172G=
XM_006711298.2:c.1379G=	XP_006711361.1:p.Ser460=
XM_017001199.2:c.1478G=	XP_016856688.1:p.Ser493=
XM_017001200.2:c.1430G=	XP_016856689.1:p.Ser477=
XM_017001201.2:c.*172G=	XP_016856690.1:n.*172G=
NM_000565.4:c.1331G= MANE Select	NP_000556.1:p.Ser444=
NM_181359.3:c.*139G=	NP_852004.1:n.*139G=
NM_001382769.1:c.1430G=	NP_001369698.1:p.Ser477=
NM_001382770.1:c.1424G=	NP_001369699.1:p.Ser475=
NM_001382771.1:c.1379G=	NP_001369700.1:p.Ser460=
NM_001382772.1:c.1325G=	NP_001369701.1:p.Ser442=
NM_001382773.1:c.*139G=	NP_001369702.1:n.*139G=
NM_001382774.1:c.971G=	NP_001369703.1:p.Ser324=