Canonical Allele Identifier: CA342628807

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437833A>T (hg19) ; chr1:g.154465357A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465357A>T , CM000663.2:g.154465357A>T	GRCh38
NC_000001.10:g.154437833A>T , CM000663.1:g.154437833A>T	GRCh37
NC_000001.9:g.152704457A>T	NCBI36
NG_012087.1:g.65165A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1384A>T MANE Select	ENSP00000357470.3:p.Thr462Ser
ENST00000344086.8:c.*192A>T	ENSP00000340589.4:n.*192A>T
ENST00000368485.7:c.1384A>T	ENSP00000357470.3:p.Thr462Ser
NM_000565.3:c.1384A>T	NP_000556.1:p.Thr462Ser
NM_181359.2:c.*192A>T	NP_852004.1:n.*192A>T
XM_005245139.1:c.*65A>T	XP_005245196.1:n.*65A>T
XM_005245140.1:c.*225A>T	XP_005245197.1:n.*225A>T
XM_006711298.1:c.1432A>T	XP_006711361.1:p.Thr478Ser
XM_005245139.2:c.*65A>T	XP_005245196.1:n.*65A>T
XM_005245140.3:c.*225A>T	XP_005245197.1:n.*225A>T
XM_006711298.2:c.1432A>T	XP_006711361.1:p.Thr478Ser
XM_017001199.2:c.1531A>T	XP_016856688.1:p.Thr511Ser
XM_017001200.2:c.1483A>T	XP_016856689.1:p.Thr495Ser
XM_017001201.2:c.*225A>T	XP_016856690.1:n.*225A>T
NM_000565.4:c.1384A>T MANE Select	NP_000556.1:p.Thr462Ser
NM_181359.3:c.*192A>T	NP_852004.1:n.*192A>T
NM_001382769.1:c.1483A>T	NP_001369698.1:p.Thr495Ser
NM_001382770.1:c.1477A>T	NP_001369699.1:p.Thr493Ser
NM_001382771.1:c.1432A>T	NP_001369700.1:p.Thr478Ser
NM_001382772.1:c.1378A>T	NP_001369701.1:p.Thr460Ser
NM_001382773.1:c.*192A>T	NP_001369702.1:n.*192A>T
NM_001382774.1:c.1024A>T	NP_001369703.1:p.Thr342Ser