Canonical Allele Identifier: CA342628706

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437800A>G (hg19) ; chr1:g.154465324A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465324A>G , CM000663.2:g.154465324A>G	GRCh38
NC_000001.10:g.154437800A>G , CM000663.1:g.154437800A>G	GRCh37
NC_000001.9:g.152704424A>G	NCBI36
NG_012087.1:g.65132A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1351A>G MANE Select	ENSP00000357470.3:p.Arg451Gly
ENST00000344086.8:c.*159A>G	ENSP00000340589.4:n.*159A>G
ENST00000368485.7:c.1351A>G	ENSP00000357470.3:p.Arg451Gly
NM_000565.3:c.1351A>G	NP_000556.1:p.Arg451Gly
NM_181359.2:c.*159A>G	NP_852004.1:n.*159A>G
XM_005245139.1:c.*32A>G	XP_005245196.1:n.*32A>G
XM_005245140.1:c.*192A>G	XP_005245197.1:n.*192A>G
XM_006711298.1:c.1399A>G	XP_006711361.1:p.Arg467Gly
XM_005245139.2:c.*32A>G	XP_005245196.1:n.*32A>G
XM_005245140.3:c.*192A>G	XP_005245197.1:n.*192A>G
XM_006711298.2:c.1399A>G	XP_006711361.1:p.Arg467Gly
XM_017001199.2:c.1498A>G	XP_016856688.1:p.Arg500Gly
XM_017001200.2:c.1450A>G	XP_016856689.1:p.Arg484Gly
XM_017001201.2:c.*192A>G	XP_016856690.1:n.*192A>G
NM_000565.4:c.1351A>G MANE Select	NP_000556.1:p.Arg451Gly
NM_181359.3:c.*159A>G	NP_852004.1:n.*159A>G
NM_001382769.1:c.1450A>G	NP_001369698.1:p.Arg484Gly
NM_001382770.1:c.1444A>G	NP_001369699.1:p.Arg482Gly
NM_001382771.1:c.1399A>G	NP_001369700.1:p.Arg467Gly
NM_001382772.1:c.1345A>G	NP_001369701.1:p.Arg449Gly
NM_001382773.1:c.*159A>G	NP_001369702.1:n.*159A>G
NM_001382774.1:c.991A>G	NP_001369703.1:p.Arg331Gly