Canonical Allele Identifier: CA342628300

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437627A>G (hg19) ; chr1:g.154465151A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465151A>G , CM000663.2:g.154465151A>G	GRCh38
NC_000001.10:g.154437627A>G , CM000663.1:g.154437627A>G	GRCh37
NC_000001.9:g.152704251A>G	NCBI36
NG_012087.1:g.64959A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1178A>G MANE Select	ENSP00000357470.3:p.Lys393Arg
ENST00000344086.8:c.1084A>G	ENSP00000340589.4:p.Ser362Gly
ENST00000368485.7:c.1178A>G	ENSP00000357470.3:p.Lys393Arg
ENST00000502679.1:n.491A>G
ENST00000507256.1:n.376A>G
NM_000565.3:c.1178A>G	NP_000556.1:p.Lys393Arg
NM_181359.2:c.1084A>G	NP_852004.1:p.Ser362Gly
XM_005245139.1:c.942A>G	XP_005245196.1:p.Glu314=
XM_005245140.1:c.*19A>G	XP_005245197.1:n.*19A>G
XM_006711298.1:c.1226A>G	XP_006711361.1:p.Lys409Arg
XM_006711299.2:c.1132A>G	XP_006711362.1:p.Ser378Gly
XM_005245139.2:c.942A>G	XP_005245196.1:p.Glu314=
XM_005245140.3:c.*19A>G	XP_005245197.1:n.*19A>G
XM_006711298.2:c.1226A>G	XP_006711361.1:p.Lys409Arg
XM_006711299.4:c.1132A>G	XP_006711362.1:p.Ser378Gly
XM_017001199.2:c.1325A>G	XP_016856688.1:p.Lys442Arg
XM_017001200.2:c.1277A>G	XP_016856689.1:p.Lys426Arg
XM_017001201.2:c.*19A>G	XP_016856690.1:n.*19A>G
NM_000565.4:c.1178A>G MANE Select	NP_000556.1:p.Lys393Arg
NM_181359.3:c.1084A>G	NP_852004.1:p.Ser362Gly
NM_001382769.1:c.1277A>G	NP_001369698.1:p.Lys426Arg
NM_001382770.1:c.1271A>G	NP_001369699.1:p.Lys424Arg
NM_001382771.1:c.1226A>G	NP_001369700.1:p.Lys409Arg
NM_001382772.1:c.1172A>G	NP_001369701.1:p.Lys391Arg
NM_001382773.1:c.1132A>G	NP_001369702.1:p.Ser378Gly
NM_001382774.1:c.818A>G	NP_001369703.1:p.Lys273Arg