Canonical Allele Identifier: CA342628377

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437641A>T (hg19) ; chr1:g.154465165A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465165A>T , CM000663.2:g.154465165A>T	GRCh38
NC_000001.10:g.154437641A>T , CM000663.1:g.154437641A>T	GRCh37
NC_000001.9:g.152704265A>T	NCBI36
NG_012087.1:g.64973A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1192A>T MANE Select	ENSP00000357470.3:p.Lys398Ter
ENST00000344086.8:c.1098A>T	ENSP00000340589.4:p.Ter366Cys
ENST00000368485.7:c.1192A>T	ENSP00000357470.3:p.Lys398Ter
ENST00000502679.1:n.505A>T
ENST00000507256.1:n.390A>T
NM_000565.3:c.1192A>T	NP_000556.1:p.Lys398Ter
NM_181359.2:c.1098A>T	NP_852004.1:p.Ter366Cys
XM_005245139.1:c.956A>T	XP_005245196.1:p.Glu319Val
XM_005245140.1:c.*33A>T	XP_005245197.1:n.*33A>T
XM_006711298.1:c.1240A>T	XP_006711361.1:p.Lys414Ter
XM_006711299.2:c.1146A>T	XP_006711362.1:p.Ter382Cys
XM_005245139.2:c.956A>T	XP_005245196.1:p.Glu319Val
XM_005245140.3:c.*33A>T	XP_005245197.1:n.*33A>T
XM_006711298.2:c.1240A>T	XP_006711361.1:p.Lys414Ter
XM_006711299.4:c.1146A>T	XP_006711362.1:p.Ter382Cys
XM_017001199.2:c.1339A>T	XP_016856688.1:p.Lys447Ter
XM_017001200.2:c.1291A>T	XP_016856689.1:p.Lys431Ter
XM_017001201.2:c.*33A>T	XP_016856690.1:n.*33A>T
NM_000565.4:c.1192A>T MANE Select	NP_000556.1:p.Lys398Ter
NM_181359.3:c.1098A>T	NP_852004.1:p.Ter366Cys
NM_001382769.1:c.1291A>T	NP_001369698.1:p.Lys431Ter
NM_001382770.1:c.1285A>T	NP_001369699.1:p.Lys429Ter
NM_001382771.1:c.1240A>T	NP_001369700.1:p.Lys414Ter
NM_001382772.1:c.1186A>T	NP_001369701.1:p.Lys396Ter
NM_001382773.1:c.1146A>T	NP_001369702.1:p.Ter382Cys
NM_001382774.1:c.832A>T	NP_001369703.1:p.Lys278Ter