Canonical Allele Identifier: CA342628584

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437738C>G (hg19) ; chr1:g.154465262C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465262C>G , CM000663.2:g.154465262C>G	GRCh38
NC_000001.10:g.154437738C>G , CM000663.1:g.154437738C>G	GRCh37
NC_000001.9:g.152704362C>G	NCBI36
NG_012087.1:g.65070C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1289C>G MANE Select	ENSP00000357470.3:p.Pro430Arg
ENST00000344086.8:c.*97C>G	ENSP00000340589.4:n.*97C>G
ENST00000368485.7:c.1289C>G	ENSP00000357470.3:p.Pro430Arg
ENST00000507256.1:n.487C>G
NM_000565.3:c.1289C>G	NP_000556.1:p.Pro430Arg
NM_181359.2:c.*97C>G	NP_852004.1:n.*97C>G
XM_005245139.1:c.1053C>G	XP_005245196.1:p.Pro351=
XM_005245140.1:c.*130C>G	XP_005245197.1:n.*130C>G
XM_006711298.1:c.1337C>G	XP_006711361.1:p.Pro446Arg
XM_005245139.2:c.1053C>G	XP_005245196.1:p.Pro351=
XM_005245140.3:c.*130C>G	XP_005245197.1:n.*130C>G
XM_006711298.2:c.1337C>G	XP_006711361.1:p.Pro446Arg
XM_017001199.2:c.1436C>G	XP_016856688.1:p.Pro479Arg
XM_017001200.2:c.1388C>G	XP_016856689.1:p.Pro463Arg
XM_017001201.2:c.*130C>G	XP_016856690.1:n.*130C>G
NM_000565.4:c.1289C>G MANE Select	NP_000556.1:p.Pro430Arg
NM_181359.3:c.*97C>G	NP_852004.1:n.*97C>G
NM_001382769.1:c.1388C>G	NP_001369698.1:p.Pro463Arg
NM_001382770.1:c.1382C>G	NP_001369699.1:p.Pro461Arg
NM_001382771.1:c.1337C>G	NP_001369700.1:p.Pro446Arg
NM_001382772.1:c.1283C>G	NP_001369701.1:p.Pro428Arg
NM_001382773.1:c.*97C>G	NP_001369702.1:n.*97C>G
NM_001382774.1:c.929C>G	NP_001369703.1:p.Pro310Arg