Canonical Allele Identifier: CA342628533

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437713C>A (hg19) ; chr1:g.154465237C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465237C>A , CM000663.2:g.154465237C>A	GRCh38
NC_000001.10:g.154437713C>A , CM000663.1:g.154437713C>A	GRCh37
NC_000001.9:g.152704337C>A	NCBI36
NG_012087.1:g.65045C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1264C>A MANE Select	ENSP00000357470.3:p.Pro422Thr
ENST00000344086.8:c.*72C>A	ENSP00000340589.4:n.*72C>A
ENST00000368485.7:c.1264C>A	ENSP00000357470.3:p.Pro422Thr
ENST00000502679.1:n.577C>A
ENST00000507256.1:n.462C>A
NM_000565.3:c.1264C>A	NP_000556.1:p.Pro422Thr
NM_181359.2:c.*72C>A	NP_852004.1:n.*72C>A
XM_005245139.1:c.1028C>A	XP_005245196.1:p.Pro343His
XM_005245140.1:c.*105C>A	XP_005245197.1:n.*105C>A
XM_006711298.1:c.1312C>A	XP_006711361.1:p.Pro438Thr
XM_006711299.2:c.*72C>A	XP_006711362.1:n.*72C>A
XM_005245139.2:c.1028C>A	XP_005245196.1:p.Pro343His
XM_005245140.3:c.*105C>A	XP_005245197.1:n.*105C>A
XM_006711298.2:c.1312C>A	XP_006711361.1:p.Pro438Thr
XM_006711299.4:c.*72C>A	XP_006711362.1:n.*72C>A
XM_017001199.2:c.1411C>A	XP_016856688.1:p.Pro471Thr
XM_017001200.2:c.1363C>A	XP_016856689.1:p.Pro455Thr
XM_017001201.2:c.*105C>A	XP_016856690.1:n.*105C>A
NM_000565.4:c.1264C>A MANE Select	NP_000556.1:p.Pro422Thr
NM_181359.3:c.*72C>A	NP_852004.1:n.*72C>A
NM_001382769.1:c.1363C>A	NP_001369698.1:p.Pro455Thr
NM_001382770.1:c.1357C>A	NP_001369699.1:p.Pro453Thr
NM_001382771.1:c.1312C>A	NP_001369700.1:p.Pro438Thr
NM_001382772.1:c.1258C>A	NP_001369701.1:p.Pro420Thr
NM_001382773.1:c.*72C>A	NP_001369702.1:n.*72C>A
NM_001382774.1:c.904C>A	NP_001369703.1:p.Pro302Thr