Canonical Allele Identifier: CA420975906

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437686C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465210C>T , CM000663.2:g.154465210C>T	GRCh38
NC_000001.10:g.154437686C>T , CM000663.1:g.154437686C>T	GRCh37
NC_000001.9:g.152704310C>T	NCBI36
NG_012087.1:g.65018C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1237C>T MANE Select	ENSP00000357470.3:p.Leu413=
ENST00000344086.8:c.*45C>T	ENSP00000340589.4:n.*45C>T
ENST00000368485.7:c.1237C>T	ENSP00000357470.3:p.Leu413=
ENST00000502679.1:n.550C>T
ENST00000507256.1:n.435C>T
NM_000565.3:c.1237C>T	NP_000556.1:p.Leu413=
NM_181359.2:c.*45C>T	NP_852004.1:n.*45C>T
XM_005245139.1:c.1001C>T	XP_005245196.1:p.Ala334Val
XM_005245140.1:c.*78C>T	XP_005245197.1:n.*78C>T
XM_006711298.1:c.1285C>T	XP_006711361.1:p.Leu429=
XM_006711299.2:c.*45C>T	XP_006711362.1:n.*45C>T
XM_005245139.2:c.1001C>T	XP_005245196.1:p.Ala334Val
XM_005245140.3:c.*78C>T	XP_005245197.1:n.*78C>T
XM_006711298.2:c.1285C>T	XP_006711361.1:p.Leu429=
XM_006711299.4:c.*45C>T	XP_006711362.1:n.*45C>T
XM_017001199.2:c.1384C>T	XP_016856688.1:p.Leu462=
XM_017001200.2:c.1336C>T	XP_016856689.1:p.Leu446=
XM_017001201.2:c.*78C>T	XP_016856690.1:n.*78C>T
NM_000565.4:c.1237C>T MANE Select	NP_000556.1:p.Leu413=
NM_181359.3:c.*45C>T	NP_852004.1:n.*45C>T
NM_001382769.1:c.1336C>T	NP_001369698.1:p.Leu446=
NM_001382770.1:c.1330C>T	NP_001369699.1:p.Leu444=
NM_001382771.1:c.1285C>T	NP_001369700.1:p.Leu429=
NM_001382772.1:c.1231C>T	NP_001369701.1:p.Leu411=
NM_001382773.1:c.*45C>T	NP_001369702.1:n.*45C>T
NM_001382774.1:c.877C>T	NP_001369703.1:p.Leu293=