Canonical Allele Identifier: CA342621613

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154420606A>G (hg19) ; chr1:g.154448130A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154448130A>G , CM000663.2:g.154448130A>G	GRCh38
NC_000001.10:g.154420606A>G , CM000663.1:g.154420606A>G	GRCh37
NC_000001.9:g.152687230A>G	NCBI36
NG_012087.1:g.47938A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368485.8:c.955A>G MANE Select	ENSP00000357470.3:p.Arg319Gly
ENST00000344086.8:c.955A>G	ENSP00000340589.4:p.Arg319Gly
ENST00000368485.7:c.955A>G	ENSP00000357470.3:p.Arg319Gly
ENST00000476006.5:c.771A>G
ENST00000507256.1:n.153A>G
ENST00000515190.1:c.363A>G
NM_000565.3:c.955A>G	NP_000556.1:p.Arg319Gly
NM_181359.2:c.955A>G	NP_852004.1:p.Arg319Gly
XM_005245139.1:c.813A>G	XP_005245196.1:p.Pro271=
XM_005245140.1:c.813A>G	XP_005245197.1:p.Pro271=
XM_006711298.1:c.1003A>G	XP_006711361.1:p.Arg335Gly
XM_006711299.2:c.1003A>G	XP_006711362.1:p.Arg335Gly
XM_005245139.2:c.813A>G	XP_005245196.1:p.Pro271=
XM_005245140.3:c.813A>G	XP_005245197.1:p.Pro271=
XM_006711298.2:c.1003A>G	XP_006711361.1:p.Arg335Gly
XM_006711299.4:c.1003A>G	XP_006711362.1:p.Arg335Gly
XM_017001199.2:c.1003A>G	XP_016856688.1:p.Arg335Gly
XM_017001200.2:c.955A>G	XP_016856689.1:p.Arg319Gly
XM_017001201.2:c.813A>G	XP_016856690.1:p.Pro271=
NM_000565.4:c.955A>G MANE Select	NP_000556.1:p.Arg319Gly
NM_181359.3:c.955A>G	NP_852004.1:p.Arg319Gly
NM_001382769.1:c.955A>G	NP_001369698.1:p.Arg319Gly
NM_001382770.1:c.1048A>G	NP_001369699.1:p.Arg350Gly
NM_001382771.1:c.1003A>G	NP_001369700.1:p.Arg335Gly
NM_001382772.1:c.949A>G	NP_001369701.1:p.Arg317Gly
NM_001382773.1:c.1003A>G	NP_001369702.1:p.Arg335Gly
NM_001382774.1:c.595A>G	NP_001369703.1:p.Arg199Gly