Canonical Allele Identifier: CA2480880320

Gene: IL6R

Linked Data

• dbSNP Id: rs1691501879

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465302_154465303insGG , CM000663.2:g.154465302_154465303insGG	GRCh38
NC_000001.10:g.154437778_154437779insGG , CM000663.1:g.154437778_154437779insGG	GRCh37
NC_000001.9:g.152704402_152704403insGG	NCBI36
NG_012087.1:g.65110_65111insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1329_1330insGG MANE Select	ENSP00000357470.3:p.Ser444GlyfsTer?
ENST00000344086.8:c.*137_*138insGG	ENSP00000340589.4:n.*137_*138insGG
ENST00000368485.7:c.1329_1330insGG	ENSP00000357470.3:p.Ser444GlyfsTer?
ENST00000507256.1:n.527_528insGG
NM_000565.3:c.1329_1330insGG	NP_000556.1:p.Ser444GlyfsTer?
NM_181359.2:c.*137_*138insGG	NP_852004.1:n.*137_*138insGG
XM_005245139.1:c.*10_*11insGG	XP_005245196.1:n.*10_*11insGG
XM_005245140.1:c.*170_*171insGG	XP_005245197.1:n.*170_*171insGG
XM_006711298.1:c.1377_1378insGG	XP_006711361.1:p.Ser460GlyfsTer?
XM_005245139.2:c.*10_*11insGG	XP_005245196.1:n.*10_*11insGG
XM_005245140.3:c.*170_*171insGG	XP_005245197.1:n.*170_*171insGG
XM_006711298.2:c.1377_1378insGG	XP_006711361.1:p.Ser460GlyfsTer?
XM_017001199.2:c.1476_1477insGG	XP_016856688.1:p.Ser493GlyfsTer?
XM_017001200.2:c.1428_1429insGG	XP_016856689.1:p.Ser477GlyfsTer?
XM_017001201.2:c.*170_*171insGG	XP_016856690.1:n.*170_*171insGG
NM_000565.4:c.1329_1330insGG MANE Select	NP_000556.1:p.Ser444GlyfsTer?
NM_181359.3:c.*137_*138insGG	NP_852004.1:n.*137_*138insGG
NM_001382769.1:c.1428_1429insGG	NP_001369698.1:p.Ser477GlyfsTer?
NM_001382770.1:c.1422_1423insGG	NP_001369699.1:p.Ser475GlyfsTer?
NM_001382771.1:c.1377_1378insGG	NP_001369700.1:p.Ser460GlyfsTer?
NM_001382772.1:c.1323_1324insGG	NP_001369701.1:p.Ser442GlyfsTer?
NM_001382773.1:c.*137_*138insGG	NP_001369702.1:n.*137_*138insGG
NM_001382774.1:c.969_970insGG	NP_001369703.1:p.Ser324GlyfsTer?