Canonical Allele Identifier: CA342628207

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437610G>C (hg19) ; chr1:g.154465134G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465134G>C , CM000663.2:g.154465134G>C	GRCh38
NC_000001.10:g.154437610G>C , CM000663.1:g.154437610G>C	GRCh37
NC_000001.9:g.152704234G>C	NCBI36
NG_012087.1:g.64942G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1161G>C MANE Select	ENSP00000357470.3:p.Arg387Ser
ENST00000344086.8:c.1067G>C	ENSP00000340589.4:p.Gly356Ala
ENST00000368485.7:c.1161G>C	ENSP00000357470.3:p.Arg387Ser
ENST00000502679.1:n.474G>C
ENST00000507256.1:n.359G>C
NM_000565.3:c.1161G>C	NP_000556.1:p.Arg387Ser
NM_181359.2:c.1067G>C	NP_852004.1:p.Gly356Ala
XM_005245139.1:c.925G>C	XP_005245196.1:p.Val309Leu
XM_005245140.1:c.*2G>C	XP_005245197.1:n.*2G>C
XM_006711298.1:c.1209G>C	XP_006711361.1:p.Arg403Ser
XM_006711299.2:c.1115G>C	XP_006711362.1:p.Gly372Ala
XM_005245139.2:c.925G>C	XP_005245196.1:p.Val309Leu
XM_005245140.3:c.*2G>C	XP_005245197.1:n.*2G>C
XM_006711298.2:c.1209G>C	XP_006711361.1:p.Arg403Ser
XM_006711299.4:c.1115G>C	XP_006711362.1:p.Gly372Ala
XM_017001199.2:c.1308G>C	XP_016856688.1:p.Arg436Ser
XM_017001200.2:c.1260G>C	XP_016856689.1:p.Arg420Ser
XM_017001201.2:c.*2G>C	XP_016856690.1:n.*2G>C
NM_000565.4:c.1161G>C MANE Select	NP_000556.1:p.Arg387Ser
NM_181359.3:c.1067G>C	NP_852004.1:p.Gly356Ala
NM_001382769.1:c.1260G>C	NP_001369698.1:p.Arg420Ser
NM_001382770.1:c.1254G>C	NP_001369699.1:p.Arg418Ser
NM_001382771.1:c.1209G>C	NP_001369700.1:p.Arg403Ser
NM_001382772.1:c.1155G>C	NP_001369701.1:p.Arg385Ser
NM_001382773.1:c.1115G>C	NP_001369702.1:p.Gly372Ala
NM_001382774.1:c.801G>C	NP_001369703.1:p.Arg267Ser