Canonical Allele Identifier: CA2480875688

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154454213C= , CM000663.2:g.154454213C=	GRCh38
NC_000001.10:g.154426689C= , CM000663.1:g.154426689C=	GRCh37
NC_000001.9:g.152693313C=	NCBI36
NG_012087.1:g.54021C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1067-275C= MANE Select	ENSP00000357470.3:n.1067-275C=
ENST00000344086.8:c.1066+4233C=	ENSP00000340589.4:n.1066+4233C=
ENST00000368485.7:c.1067-275C=	ENSP00000357470.3:n.1067-275C=
ENST00000502679.1:n.105C=
ENST00000507256.1:n.265-275C=
ENST00000515190.1:c.475-275C=
NM_000565.3:c.1067-275C=	NP_000556.1:n.1067-275C=
NM_181359.2:c.1066+4233C=	NP_852004.1:n.1066+4233C=
XM_005245139.1:c.924+4233C=	XP_005245196.1:n.924+4233C=
XM_005245140.1:c.925-275C=	XP_005245197.1:n.925-275C=
XM_006711298.1:c.1115-275C=	XP_006711361.1:n.1115-275C=
XM_006711299.2:c.1114+4233C=	XP_006711362.1:n.1114+4233C=
XM_005245139.2:c.924+4233C=	XP_005245196.1:n.924+4233C=
XM_005245140.3:c.925-275C=	XP_005245197.1:n.925-275C=
XM_006711298.2:c.1115-275C=	XP_006711361.1:n.1115-275C=
XM_006711299.4:c.1114+4233C=	XP_006711362.1:n.1114+4233C=
XM_017001199.2:c.1213+42C=	XP_016856688.1:n.1213+42C=
XM_017001200.2:c.1165+42C=	XP_016856689.1:n.1165+42C=
XM_017001201.2:c.1023+42C=	XP_016856690.1:n.1023+42C=
NM_000565.4:c.1067-275C= MANE Select	NP_000556.1:n.1067-275C=
NM_181359.3:c.1066+4233C=	NP_852004.1:n.1066+4233C=
NM_001382769.1:c.1165+42C=	NP_001369698.1:n.1165+42C=
NM_001382770.1:c.1160-275C=	NP_001369699.1:n.1160-275C=
NM_001382771.1:c.1115-275C=	NP_001369700.1:n.1115-275C=
NM_001382772.1:c.1061-275C=	NP_001369701.1:n.1061-275C=
NM_001382773.1:c.1114+4233C=	NP_001369702.1:n.1114+4233C=
NM_001382774.1:c.707-275C=	NP_001369703.1:n.707-275C=