Canonical Allele Identifier: CA420975890

Gene: IL6R

Linked Data

• dbSNP Id: rs1691492671
• MyVariant Identifiers: chr1:g.154437676T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465200T>C , CM000663.2:g.154465200T>C	GRCh38
NC_000001.10:g.154437676T>C , CM000663.1:g.154437676T>C	GRCh37
NC_000001.9:g.152704300T>C	NCBI36
NG_012087.1:g.65008T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1227T>C MANE Select	ENSP00000357470.3:p.Ser409=
ENST00000344086.8:c.*35T>C	ENSP00000340589.4:n.*35T>C
ENST00000368485.7:c.1227T>C	ENSP00000357470.3:p.Ser409=
ENST00000502679.1:n.540T>C
ENST00000507256.1:n.425T>C
NM_000565.3:c.1227T>C	NP_000556.1:p.Ser409=
NM_181359.2:c.*35T>C	NP_852004.1:n.*35T>C
XM_005245139.1:c.991T>C	XP_005245196.1:p.Phe331Leu
XM_005245140.1:c.*68T>C	XP_005245197.1:n.*68T>C
XM_006711298.1:c.1275T>C	XP_006711361.1:p.Ser425=
XM_006711299.2:c.*35T>C	XP_006711362.1:n.*35T>C
XM_005245139.2:c.991T>C	XP_005245196.1:p.Phe331Leu
XM_005245140.3:c.*68T>C	XP_005245197.1:n.*68T>C
XM_006711298.2:c.1275T>C	XP_006711361.1:p.Ser425=
XM_006711299.4:c.*35T>C	XP_006711362.1:n.*35T>C
XM_017001199.2:c.1374T>C	XP_016856688.1:p.Ser458=
XM_017001200.2:c.1326T>C	XP_016856689.1:p.Ser442=
XM_017001201.2:c.*68T>C	XP_016856690.1:n.*68T>C
NM_000565.4:c.1227T>C MANE Select	NP_000556.1:p.Ser409=
NM_181359.3:c.*35T>C	NP_852004.1:n.*35T>C
NM_001382769.1:c.1326T>C	NP_001369698.1:p.Ser442=
NM_001382770.1:c.1320T>C	NP_001369699.1:p.Ser440=
NM_001382771.1:c.1275T>C	NP_001369700.1:p.Ser425=
NM_001382772.1:c.1221T>C	NP_001369701.1:p.Ser407=
NM_001382773.1:c.*35T>C	NP_001369702.1:n.*35T>C
NM_001382774.1:c.867T>C	NP_001369703.1:p.Ser289=