Canonical Allele Identifier: CA2480880258

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465152G= , CM000663.2:g.154465152G=	GRCh38
NC_000001.10:g.154437628G= , CM000663.1:g.154437628G=	GRCh37
NC_000001.9:g.152704252G=	NCBI36
NG_012087.1:g.64960G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1179G= MANE Select	ENSP00000357470.3:p.Lys393=
ENST00000344086.8:c.1085G=	ENSP00000340589.4:p.Ser362=
ENST00000368485.7:c.1179G=	ENSP00000357470.3:p.Lys393=
ENST00000502679.1:n.492G=
ENST00000507256.1:n.377G=
NM_000565.3:c.1179G=	NP_000556.1:p.Lys393=
NM_181359.2:c.1085G=	NP_852004.1:p.Ser362=
XM_005245139.1:c.943G=	XP_005245196.1:p.Ala315=
XM_005245140.1:c.*20G=	XP_005245197.1:n.*20G=
XM_006711298.1:c.1227G=	XP_006711361.1:p.Lys409=
XM_006711299.2:c.1133G=	XP_006711362.1:p.Ser378=
XM_005245139.2:c.943G=	XP_005245196.1:p.Ala315=
XM_005245140.3:c.*20G=	XP_005245197.1:n.*20G=
XM_006711298.2:c.1227G=	XP_006711361.1:p.Lys409=
XM_006711299.4:c.1133G=	XP_006711362.1:p.Ser378=
XM_017001199.2:c.1326G=	XP_016856688.1:p.Lys442=
XM_017001200.2:c.1278G=	XP_016856689.1:p.Lys426=
XM_017001201.2:c.*20G=	XP_016856690.1:n.*20G=
NM_000565.4:c.1179G= MANE Select	NP_000556.1:p.Lys393=
NM_181359.3:c.1085G=	NP_852004.1:p.Ser362=
NM_001382769.1:c.1278G=	NP_001369698.1:p.Lys426=
NM_001382770.1:c.1272G=	NP_001369699.1:p.Lys424=
NM_001382771.1:c.1227G=	NP_001369700.1:p.Lys409=
NM_001382772.1:c.1173G=	NP_001369701.1:p.Lys391=
NM_001382773.1:c.1133G=	NP_001369702.1:p.Ser378=
NM_001382774.1:c.819G=	NP_001369703.1:p.Lys273=