Canonical Allele Identifier: CA420974969

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154420617A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154448141A>G , CM000663.2:g.154448141A>G	GRCh38
NC_000001.10:g.154420617A>G , CM000663.1:g.154420617A>G	GRCh37
NC_000001.9:g.152687241A>G	NCBI36
NG_012087.1:g.47949A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368485.8:c.966A>G MANE Select	ENSP00000357470.3:p.Pro322=
ENST00000344086.8:c.966A>G	ENSP00000340589.4:p.Pro322=
ENST00000368485.7:c.966A>G	ENSP00000357470.3:p.Pro322=
ENST00000476006.5:c.782A>G
ENST00000507256.1:n.164A>G
ENST00000515190.1:c.374A>G
NM_000565.3:c.966A>G	NP_000556.1:p.Pro322=
NM_181359.2:c.966A>G	NP_852004.1:p.Pro322=
XM_005245139.1:c.824A>G	XP_005245196.1:p.Gln275Arg
XM_005245140.1:c.824A>G	XP_005245197.1:p.Gln275Arg
XM_006711298.1:c.1014A>G	XP_006711361.1:p.Pro338=
XM_006711299.2:c.1014A>G	XP_006711362.1:p.Pro338=
XM_005245139.2:c.824A>G	XP_005245196.1:p.Gln275Arg
XM_005245140.3:c.824A>G	XP_005245197.1:p.Gln275Arg
XM_006711298.2:c.1014A>G	XP_006711361.1:p.Pro338=
XM_006711299.4:c.1014A>G	XP_006711362.1:p.Pro338=
XM_017001199.2:c.1014A>G	XP_016856688.1:p.Pro338=
XM_017001200.2:c.966A>G	XP_016856689.1:p.Pro322=
XM_017001201.2:c.824A>G	XP_016856690.1:p.Gln275Arg
NM_000565.4:c.966A>G MANE Select	NP_000556.1:p.Pro322=
NM_181359.3:c.966A>G	NP_852004.1:p.Pro322=
NM_001382769.1:c.966A>G	NP_001369698.1:p.Pro322=
NM_001382770.1:c.1059A>G	NP_001369699.1:p.Pro353=
NM_001382771.1:c.1014A>G	NP_001369700.1:p.Pro338=
NM_001382772.1:c.960A>G	NP_001369701.1:p.Pro320=
NM_001382773.1:c.1014A>G	NP_001369702.1:p.Pro338=
NM_001382774.1:c.606A>G	NP_001369703.1:p.Pro202=