Canonical Allele Identifier: CA342628296

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437626A>T (hg19) ; chr1:g.154465150A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465150A>T , CM000663.2:g.154465150A>T	GRCh38
NC_000001.10:g.154437626A>T , CM000663.1:g.154437626A>T	GRCh37
NC_000001.9:g.152704250A>T	NCBI36
NG_012087.1:g.64958A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1177A>T MANE Select	ENSP00000357470.3:p.Lys393Ter
ENST00000344086.8:c.1083A>T	ENSP00000340589.4:p.Gly361=
ENST00000368485.7:c.1177A>T	ENSP00000357470.3:p.Lys393Ter
ENST00000502679.1:n.490A>T
ENST00000507256.1:n.375A>T
NM_000565.3:c.1177A>T	NP_000556.1:p.Lys393Ter
NM_181359.2:c.1083A>T	NP_852004.1:p.Gly361=
XM_005245139.1:c.941A>T	XP_005245196.1:p.Glu314Val
XM_005245140.1:c.*18A>T	XP_005245197.1:n.*18A>T
XM_006711298.1:c.1225A>T	XP_006711361.1:p.Lys409Ter
XM_006711299.2:c.1131A>T	XP_006711362.1:p.Gly377=
XM_005245139.2:c.941A>T	XP_005245196.1:p.Glu314Val
XM_005245140.3:c.*18A>T	XP_005245197.1:n.*18A>T
XM_006711298.2:c.1225A>T	XP_006711361.1:p.Lys409Ter
XM_006711299.4:c.1131A>T	XP_006711362.1:p.Gly377=
XM_017001199.2:c.1324A>T	XP_016856688.1:p.Lys442Ter
XM_017001200.2:c.1276A>T	XP_016856689.1:p.Lys426Ter
XM_017001201.2:c.*18A>T	XP_016856690.1:n.*18A>T
NM_000565.4:c.1177A>T MANE Select	NP_000556.1:p.Lys393Ter
NM_181359.3:c.1083A>T	NP_852004.1:p.Gly361=
NM_001382769.1:c.1276A>T	NP_001369698.1:p.Lys426Ter
NM_001382770.1:c.1270A>T	NP_001369699.1:p.Lys424Ter
NM_001382771.1:c.1225A>T	NP_001369700.1:p.Lys409Ter
NM_001382772.1:c.1171A>T	NP_001369701.1:p.Lys391Ter
NM_001382773.1:c.1131A>T	NP_001369702.1:p.Gly377=
NM_001382774.1:c.817A>T	NP_001369703.1:p.Lys273Ter