Canonical Allele Identifier: CA420975868

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437655A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465179A>T , CM000663.2:g.154465179A>T	GRCh38
NC_000001.10:g.154437655A>T , CM000663.1:g.154437655A>T	GRCh37
NC_000001.9:g.152704279A>T	NCBI36
NG_012087.1:g.64987A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1206A>T MANE Select	ENSP00000357470.3:p.Thr402=
ENST00000344086.8:c.*14A>T	ENSP00000340589.4:n.*14A>T
ENST00000368485.7:c.1206A>T	ENSP00000357470.3:p.Thr402=
ENST00000502679.1:n.519A>T
ENST00000507256.1:n.404A>T
NM_000565.3:c.1206A>T	NP_000556.1:p.Thr402=
NM_181359.2:c.*14A>T	NP_852004.1:n.*14A>T
XM_005245139.1:c.970A>T	XP_005245196.1:p.Lys324Ter
XM_005245140.1:c.*47A>T	XP_005245197.1:n.*47A>T
XM_006711298.1:c.1254A>T	XP_006711361.1:p.Thr418=
XM_006711299.2:c.*14A>T	XP_006711362.1:n.*14A>T
XM_005245139.2:c.970A>T	XP_005245196.1:p.Lys324Ter
XM_005245140.3:c.*47A>T	XP_005245197.1:n.*47A>T
XM_006711298.2:c.1254A>T	XP_006711361.1:p.Thr418=
XM_006711299.4:c.*14A>T	XP_006711362.1:n.*14A>T
XM_017001199.2:c.1353A>T	XP_016856688.1:p.Thr451=
XM_017001200.2:c.1305A>T	XP_016856689.1:p.Thr435=
XM_017001201.2:c.*47A>T	XP_016856690.1:n.*47A>T
NM_000565.4:c.1206A>T MANE Select	NP_000556.1:p.Thr402=
NM_181359.3:c.*14A>T	NP_852004.1:n.*14A>T
NM_001382769.1:c.1305A>T	NP_001369698.1:p.Thr435=
NM_001382770.1:c.1299A>T	NP_001369699.1:p.Thr433=
NM_001382771.1:c.1254A>T	NP_001369700.1:p.Thr418=
NM_001382772.1:c.1200A>T	NP_001369701.1:p.Thr400=
NM_001382773.1:c.*14A>T	NP_001369702.1:n.*14A>T
NM_001382774.1:c.846A>T	NP_001369703.1:p.Thr282=