Canonical Allele Identifier: CA420975859

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437649C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465173C>A , CM000663.2:g.154465173C>A	GRCh38
NC_000001.10:g.154437649C>A , CM000663.1:g.154437649C>A	GRCh37
NC_000001.9:g.152704273C>A	NCBI36
NG_012087.1:g.64981C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1200C>A MANE Select	ENSP00000357470.3:p.Gly400=
ENST00000344086.8:c.*8C>A	ENSP00000340589.4:n.*8C>A
ENST00000368485.7:c.1200C>A	ENSP00000357470.3:p.Gly400=
ENST00000502679.1:n.513C>A
ENST00000507256.1:n.398C>A
NM_000565.3:c.1200C>A	NP_000556.1:p.Gly400=
NM_181359.2:c.*8C>A	NP_852004.1:n.*8C>A
XM_005245139.1:c.964C>A	XP_005245196.1:p.Gln322Lys
XM_005245140.1:c.*41C>A	XP_005245197.1:n.*41C>A
XM_006711298.1:c.1248C>A	XP_006711361.1:p.Gly416=
XM_006711299.2:c.*8C>A	XP_006711362.1:n.*8C>A
XM_005245139.2:c.964C>A	XP_005245196.1:p.Gln322Lys
XM_005245140.3:c.*41C>A	XP_005245197.1:n.*41C>A
XM_006711298.2:c.1248C>A	XP_006711361.1:p.Gly416=
XM_006711299.4:c.*8C>A	XP_006711362.1:n.*8C>A
XM_017001199.2:c.1347C>A	XP_016856688.1:p.Gly449=
XM_017001200.2:c.1299C>A	XP_016856689.1:p.Gly433=
XM_017001201.2:c.*41C>A	XP_016856690.1:n.*41C>A
NM_000565.4:c.1200C>A MANE Select	NP_000556.1:p.Gly400=
NM_181359.3:c.*8C>A	NP_852004.1:n.*8C>A
NM_001382769.1:c.1299C>A	NP_001369698.1:p.Gly433=
NM_001382770.1:c.1293C>A	NP_001369699.1:p.Gly431=
NM_001382771.1:c.1248C>A	NP_001369700.1:p.Gly416=
NM_001382772.1:c.1194C>A	NP_001369701.1:p.Gly398=
NM_001382773.1:c.*8C>A	NP_001369702.1:n.*8C>A
NM_001382774.1:c.840C>A	NP_001369703.1:p.Gly280=