Canonical Allele Identifier: CA342628535

Gene: IL6R

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1264C>G MANE Select	ENSP00000357470.3:p.Pro422Ala
ENST00000344086.8:c.*72C>G	ENSP00000340589.4:n.*72C>G
ENST00000368485.7:c.1264C>G	ENSP00000357470.3:p.Pro422Ala
ENST00000502679.1:n.577C>G
ENST00000507256.1:n.462C>G
NM_000565.3:c.1264C>G	NP_000556.1:p.Pro422Ala
NM_181359.2:c.*72C>G	NP_852004.1:n.*72C>G
XM_005245139.1:c.1028C>G	XP_005245196.1:p.Pro343Arg
XM_005245140.1:c.*105C>G	XP_005245197.1:n.*105C>G
XM_006711298.1:c.1312C>G	XP_006711361.1:p.Pro438Ala
XM_006711299.2:c.*72C>G	XP_006711362.1:n.*72C>G
XM_005245139.2:c.1028C>G	XP_005245196.1:p.Pro343Arg
XM_005245140.3:c.*105C>G	XP_005245197.1:n.*105C>G
XM_006711298.2:c.1312C>G	XP_006711361.1:p.Pro438Ala
XM_006711299.4:c.*72C>G	XP_006711362.1:n.*72C>G
XM_017001199.2:c.1411C>G	XP_016856688.1:p.Pro471Ala
XM_017001200.2:c.1363C>G	XP_016856689.1:p.Pro455Ala
XM_017001201.2:c.*105C>G	XP_016856690.1:n.*105C>G
NM_000565.4:c.1264C>G MANE Select	NP_000556.1:p.Pro422Ala
NM_181359.3:c.*72C>G	NP_852004.1:n.*72C>G
NM_001382769.1:c.1363C>G	NP_001369698.1:p.Pro455Ala
NM_001382770.1:c.1357C>G	NP_001369699.1:p.Pro453Ala
NM_001382771.1:c.1312C>G	NP_001369700.1:p.Pro438Ala
NM_001382772.1:c.1258C>G	NP_001369701.1:p.Pro420Ala
NM_001382773.1:c.*72C>G	NP_001369702.1:n.*72C>G
NM_001382774.1:c.904C>G	NP_001369703.1:p.Pro302Ala