Canonical Allele Identifier: CA2480880349

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465364A= , CM000663.2:g.154465364A=	GRCh38
NC_000001.10:g.154437840A= , CM000663.1:g.154437840A=	GRCh37
NC_000001.9:g.152704464A=	NCBI36
NG_012087.1:g.65172A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1391A= MANE Select	ENSP00000357470.3:p.Tyr464=
ENST00000344086.8:c.*199A=	ENSP00000340589.4:n.*199A=
ENST00000368485.7:c.1391A=	ENSP00000357470.3:p.Tyr464=
NM_000565.3:c.1391A=	NP_000556.1:p.Tyr464=
NM_181359.2:c.*199A=	NP_852004.1:n.*199A=
XM_005245139.1:c.*72A=	XP_005245196.1:n.*72A=
XM_005245140.1:c.*232A=	XP_005245197.1:n.*232A=
XM_006711298.1:c.1439A=	XP_006711361.1:p.Tyr480=
XM_005245139.2:c.*72A=	XP_005245196.1:n.*72A=
XM_005245140.3:c.*232A=	XP_005245197.1:n.*232A=
XM_006711298.2:c.1439A=	XP_006711361.1:p.Tyr480=
XM_017001199.2:c.1538A=	XP_016856688.1:p.Tyr513=
XM_017001200.2:c.1490A=	XP_016856689.1:p.Tyr497=
XM_017001201.2:c.*232A=	XP_016856690.1:n.*232A=
NM_000565.4:c.1391A= MANE Select	NP_000556.1:p.Tyr464=
NM_181359.3:c.*199A=	NP_852004.1:n.*199A=
NM_001382769.1:c.1490A=	NP_001369698.1:p.Tyr497=
NM_001382770.1:c.1484A=	NP_001369699.1:p.Tyr495=
NM_001382771.1:c.1439A=	NP_001369700.1:p.Tyr480=
NM_001382772.1:c.1385A=	NP_001369701.1:p.Tyr462=
NM_001382773.1:c.*199A=	NP_001369702.1:n.*199A=
NM_001382774.1:c.1031A=	NP_001369703.1:p.Tyr344=