Canonical Allele Identifier: CA342628389

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437645A>G (hg19) ; chr1:g.154465169A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465169A>G , CM000663.2:g.154465169A>G	GRCh38
NC_000001.10:g.154437645A>G , CM000663.1:g.154437645A>G	GRCh37
NC_000001.9:g.152704269A>G	NCBI36
NG_012087.1:g.64977A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1196A>G MANE Select	ENSP00000357470.3:p.Glu399Gly
ENST00000344086.8:c.*4A>G	ENSP00000340589.4:n.*4A>G
ENST00000368485.7:c.1196A>G	ENSP00000357470.3:p.Glu399Gly
ENST00000502679.1:n.509A>G
ENST00000507256.1:n.394A>G
NM_000565.3:c.1196A>G	NP_000556.1:p.Glu399Gly
NM_181359.2:c.*4A>G	NP_852004.1:n.*4A>G
XM_005245139.1:c.960A>G	XP_005245196.1:p.Gly320=
XM_005245140.1:c.*37A>G	XP_005245197.1:n.*37A>G
XM_006711298.1:c.1244A>G	XP_006711361.1:p.Glu415Gly
XM_006711299.2:c.*4A>G	XP_006711362.1:n.*4A>G
XM_005245139.2:c.960A>G	XP_005245196.1:p.Gly320=
XM_005245140.3:c.*37A>G	XP_005245197.1:n.*37A>G
XM_006711298.2:c.1244A>G	XP_006711361.1:p.Glu415Gly
XM_006711299.4:c.*4A>G	XP_006711362.1:n.*4A>G
XM_017001199.2:c.1343A>G	XP_016856688.1:p.Glu448Gly
XM_017001200.2:c.1295A>G	XP_016856689.1:p.Glu432Gly
XM_017001201.2:c.*37A>G	XP_016856690.1:n.*37A>G
NM_000565.4:c.1196A>G MANE Select	NP_000556.1:p.Glu399Gly
NM_181359.3:c.*4A>G	NP_852004.1:n.*4A>G
NM_001382769.1:c.1295A>G	NP_001369698.1:p.Glu432Gly
NM_001382770.1:c.1289A>G	NP_001369699.1:p.Glu430Gly
NM_001382771.1:c.1244A>G	NP_001369700.1:p.Glu415Gly
NM_001382772.1:c.1190A>G	NP_001369701.1:p.Glu397Gly
NM_001382773.1:c.*4A>G	NP_001369702.1:n.*4A>G
NM_001382774.1:c.836A>G	NP_001369703.1:p.Glu279Gly