Canonical Allele Identifier: CA342628391

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437646A>C (hg19) ; chr1:g.154465170A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465170A>C , CM000663.2:g.154465170A>C	GRCh38
NC_000001.10:g.154437646A>C , CM000663.1:g.154437646A>C	GRCh37
NC_000001.9:g.152704270A>C	NCBI36
NG_012087.1:g.64978A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1197A>C MANE Select	ENSP00000357470.3:p.Glu399Asp
ENST00000344086.8:c.*5A>C	ENSP00000340589.4:n.*5A>C
ENST00000368485.7:c.1197A>C	ENSP00000357470.3:p.Glu399Asp
ENST00000502679.1:n.510A>C
ENST00000507256.1:n.395A>C
NM_000565.3:c.1197A>C	NP_000556.1:p.Glu399Asp
NM_181359.2:c.*5A>C	NP_852004.1:n.*5A>C
XM_005245139.1:c.961A>C	XP_005245196.1:p.Arg321=
XM_005245140.1:c.*38A>C	XP_005245197.1:n.*38A>C
XM_006711298.1:c.1245A>C	XP_006711361.1:p.Glu415Asp
XM_006711299.2:c.*5A>C	XP_006711362.1:n.*5A>C
XM_005245139.2:c.961A>C	XP_005245196.1:p.Arg321=
XM_005245140.3:c.*38A>C	XP_005245197.1:n.*38A>C
XM_006711298.2:c.1245A>C	XP_006711361.1:p.Glu415Asp
XM_006711299.4:c.*5A>C	XP_006711362.1:n.*5A>C
XM_017001199.2:c.1344A>C	XP_016856688.1:p.Glu448Asp
XM_017001200.2:c.1296A>C	XP_016856689.1:p.Glu432Asp
XM_017001201.2:c.*38A>C	XP_016856690.1:n.*38A>C
NM_000565.4:c.1197A>C MANE Select	NP_000556.1:p.Glu399Asp
NM_181359.3:c.*5A>C	NP_852004.1:n.*5A>C
NM_001382769.1:c.1296A>C	NP_001369698.1:p.Glu432Asp
NM_001382770.1:c.1290A>C	NP_001369699.1:p.Glu430Asp
NM_001382771.1:c.1245A>C	NP_001369700.1:p.Glu415Asp
NM_001382772.1:c.1191A>C	NP_001369701.1:p.Glu397Asp
NM_001382773.1:c.*5A>C	NP_001369702.1:n.*5A>C
NM_001382774.1:c.837A>C	NP_001369703.1:p.Glu279Asp