Canonical Allele Identifier: CA342628282

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437624G>C (hg19) ; chr1:g.154465148G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465148G>C , CM000663.2:g.154465148G>C	GRCh38
NC_000001.10:g.154437624G>C , CM000663.1:g.154437624G>C	GRCh37
NC_000001.9:g.152704248G>C	NCBI36
NG_012087.1:g.64956G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1175G>C MANE Select	ENSP00000357470.3:p.Trp392Ser
ENST00000344086.8:c.1081G>C	ENSP00000340589.4:p.Gly361Arg
ENST00000368485.7:c.1175G>C	ENSP00000357470.3:p.Trp392Ser
ENST00000502679.1:n.488G>C
ENST00000507256.1:n.373G>C
NM_000565.3:c.1175G>C	NP_000556.1:p.Trp392Ser
NM_181359.2:c.1081G>C	NP_852004.1:p.Gly361Arg
XM_005245139.1:c.939G>C	XP_005245196.1:p.Val313=
XM_005245140.1:c.*16G>C	XP_005245197.1:n.*16G>C
XM_006711298.1:c.1223G>C	XP_006711361.1:p.Trp408Ser
XM_006711299.2:c.1129G>C	XP_006711362.1:p.Gly377Arg
XM_005245139.2:c.939G>C	XP_005245196.1:p.Val313=
XM_005245140.3:c.*16G>C	XP_005245197.1:n.*16G>C
XM_006711298.2:c.1223G>C	XP_006711361.1:p.Trp408Ser
XM_006711299.4:c.1129G>C	XP_006711362.1:p.Gly377Arg
XM_017001199.2:c.1322G>C	XP_016856688.1:p.Trp441Ser
XM_017001200.2:c.1274G>C	XP_016856689.1:p.Trp425Ser
XM_017001201.2:c.*16G>C	XP_016856690.1:n.*16G>C
NM_000565.4:c.1175G>C MANE Select	NP_000556.1:p.Trp392Ser
NM_181359.3:c.1081G>C	NP_852004.1:p.Gly361Arg
NM_001382769.1:c.1274G>C	NP_001369698.1:p.Trp425Ser
NM_001382770.1:c.1268G>C	NP_001369699.1:p.Trp423Ser
NM_001382771.1:c.1223G>C	NP_001369700.1:p.Trp408Ser
NM_001382772.1:c.1169G>C	NP_001369701.1:p.Trp390Ser
NM_001382773.1:c.1129G>C	NP_001369702.1:p.Gly377Arg
NM_001382774.1:c.815G>C	NP_001369703.1:p.Trp272Ser