Canonical Allele Identifier: CA420975925

Gene: IL6R

Linked Data

• gnomAD v4: 1-154465224-G-A
• MyVariant Identifiers: chr1:g.154437700G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465224G>A , CM000663.2:g.154465224G>A	GRCh38
NC_000001.10:g.154437700G>A , CM000663.1:g.154437700G>A	GRCh37
NC_000001.9:g.152704324G>A	NCBI36
NG_012087.1:g.65032G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1251G>A MANE Select	ENSP00000357470.3:p.Arg417=
ENST00000344086.8:c.*59G>A	ENSP00000340589.4:n.*59G>A
ENST00000368485.7:c.1251G>A	ENSP00000357470.3:p.Arg417=
ENST00000502679.1:n.564G>A
ENST00000507256.1:n.449G>A
NM_000565.3:c.1251G>A	NP_000556.1:p.Arg417=
NM_181359.2:c.*59G>A	NP_852004.1:n.*59G>A
XM_005245139.1:c.1015G>A	XP_005245196.1:p.Ala339Thr
XM_005245140.1:c.*92G>A	XP_005245197.1:n.*92G>A
XM_006711298.1:c.1299G>A	XP_006711361.1:p.Arg433=
XM_006711299.2:c.*59G>A	XP_006711362.1:n.*59G>A
XM_005245139.2:c.1015G>A	XP_005245196.1:p.Ala339Thr
XM_005245140.3:c.*92G>A	XP_005245197.1:n.*92G>A
XM_006711298.2:c.1299G>A	XP_006711361.1:p.Arg433=
XM_006711299.4:c.*59G>A	XP_006711362.1:n.*59G>A
XM_017001199.2:c.1398G>A	XP_016856688.1:p.Arg466=
XM_017001200.2:c.1350G>A	XP_016856689.1:p.Arg450=
XM_017001201.2:c.*92G>A	XP_016856690.1:n.*92G>A
NM_000565.4:c.1251G>A MANE Select	NP_000556.1:p.Arg417=
NM_181359.3:c.*59G>A	NP_852004.1:n.*59G>A
NM_001382769.1:c.1350G>A	NP_001369698.1:p.Arg450=
NM_001382770.1:c.1344G>A	NP_001369699.1:p.Arg448=
NM_001382771.1:c.1299G>A	NP_001369700.1:p.Arg433=
NM_001382772.1:c.1245G>A	NP_001369701.1:p.Arg415=
NM_001382773.1:c.*59G>A	NP_001369702.1:n.*59G>A
NM_001382774.1:c.891G>A	NP_001369703.1:p.Arg297=