Canonical Allele Identifier: CA420975899

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437682G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465206G>C , CM000663.2:g.154465206G>C	GRCh38
NC_000001.10:g.154437682G>C , CM000663.1:g.154437682G>C	GRCh37
NC_000001.9:g.152704306G>C	NCBI36
NG_012087.1:g.65014G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1233G>C MANE Select	ENSP00000357470.3:p.Gly411=
ENST00000344086.8:c.*41G>C	ENSP00000340589.4:n.*41G>C
ENST00000368485.7:c.1233G>C	ENSP00000357470.3:p.Gly411=
ENST00000502679.1:n.546G>C
ENST00000507256.1:n.431G>C
NM_000565.3:c.1233G>C	NP_000556.1:p.Gly411=
NM_181359.2:c.*41G>C	NP_852004.1:n.*41G>C
XM_005245139.1:c.997G>C	XP_005245196.1:p.Ala333Pro
XM_005245140.1:c.*74G>C	XP_005245197.1:n.*74G>C
XM_006711298.1:c.1281G>C	XP_006711361.1:p.Gly427=
XM_006711299.2:c.*41G>C	XP_006711362.1:n.*41G>C
XM_005245139.2:c.997G>C	XP_005245196.1:p.Ala333Pro
XM_005245140.3:c.*74G>C	XP_005245197.1:n.*74G>C
XM_006711298.2:c.1281G>C	XP_006711361.1:p.Gly427=
XM_006711299.4:c.*41G>C	XP_006711362.1:n.*41G>C
XM_017001199.2:c.1380G>C	XP_016856688.1:p.Gly460=
XM_017001200.2:c.1332G>C	XP_016856689.1:p.Gly444=
XM_017001201.2:c.*74G>C	XP_016856690.1:n.*74G>C
NM_000565.4:c.1233G>C MANE Select	NP_000556.1:p.Gly411=
NM_181359.3:c.*41G>C	NP_852004.1:n.*41G>C
NM_001382769.1:c.1332G>C	NP_001369698.1:p.Gly444=
NM_001382770.1:c.1326G>C	NP_001369699.1:p.Gly442=
NM_001382771.1:c.1281G>C	NP_001369700.1:p.Gly427=
NM_001382772.1:c.1227G>C	NP_001369701.1:p.Gly409=
NM_001382773.1:c.*41G>C	NP_001369702.1:n.*41G>C
NM_001382774.1:c.873G>C	NP_001369703.1:p.Gly291=