Canonical Allele Identifier: CA342628343

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437634G>A (hg19) ; chr1:g.154465158G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465158G>A , CM000663.2:g.154465158G>A	GRCh38
NC_000001.10:g.154437634G>A , CM000663.1:g.154437634G>A	GRCh37
NC_000001.9:g.152704258G>A	NCBI36
NG_012087.1:g.64966G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1185G>A MANE Select	ENSP00000357470.3:p.Arg395=
ENST00000344086.8:c.1091G>A	ENSP00000340589.4:p.Gly364Glu
ENST00000368485.7:c.1185G>A	ENSP00000357470.3:p.Arg395=
ENST00000502679.1:n.498G>A
ENST00000507256.1:n.383G>A
NM_000565.3:c.1185G>A	NP_000556.1:p.Arg395=
NM_181359.2:c.1091G>A	NP_852004.1:p.Gly364Glu
XM_005245139.1:c.949G>A	XP_005245196.1:p.Gly317Ser
XM_005245140.1:c.*26G>A	XP_005245197.1:n.*26G>A
XM_006711298.1:c.1233G>A	XP_006711361.1:p.Arg411=
XM_006711299.2:c.1139G>A	XP_006711362.1:p.Gly380Glu
XM_005245139.2:c.949G>A	XP_005245196.1:p.Gly317Ser
XM_005245140.3:c.*26G>A	XP_005245197.1:n.*26G>A
XM_006711298.2:c.1233G>A	XP_006711361.1:p.Arg411=
XM_006711299.4:c.1139G>A	XP_006711362.1:p.Gly380Glu
XM_017001199.2:c.1332G>A	XP_016856688.1:p.Arg444=
XM_017001200.2:c.1284G>A	XP_016856689.1:p.Arg428=
XM_017001201.2:c.*26G>A	XP_016856690.1:n.*26G>A
NM_000565.4:c.1185G>A MANE Select	NP_000556.1:p.Arg395=
NM_181359.3:c.1091G>A	NP_852004.1:p.Gly364Glu
NM_001382769.1:c.1284G>A	NP_001369698.1:p.Arg428=
NM_001382770.1:c.1278G>A	NP_001369699.1:p.Arg426=
NM_001382771.1:c.1233G>A	NP_001369700.1:p.Arg411=
NM_001382772.1:c.1179G>A	NP_001369701.1:p.Arg393=
NM_001382773.1:c.1139G>A	NP_001369702.1:p.Gly380Glu
NM_001382774.1:c.825G>A	NP_001369703.1:p.Arg275=