Canonical Allele Identifier: CA342621899

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154420636A>G (hg19) ; chr1:g.154448160A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154448160A>G , CM000663.2:g.154448160A>G	GRCh38
NC_000001.10:g.154420636A>G , CM000663.1:g.154420636A>G	GRCh37
NC_000001.9:g.152687260A>G	NCBI36
NG_012087.1:g.47968A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368485.8:c.985A>G MANE Select	ENSP00000357470.3:p.Thr329Ala
ENST00000344086.8:c.985A>G	ENSP00000340589.4:p.Thr329Ala
ENST00000368485.7:c.985A>G	ENSP00000357470.3:p.Thr329Ala
ENST00000476006.5:c.801A>G
ENST00000507256.1:n.183A>G
ENST00000515190.1:c.393A>G
NM_000565.3:c.985A>G	NP_000556.1:p.Thr329Ala
NM_181359.2:c.985A>G	NP_852004.1:p.Thr329Ala
XM_005245139.1:c.843A>G	XP_005245196.1:p.Pro281=
XM_005245140.1:c.843A>G	XP_005245197.1:p.Pro281=
XM_006711298.1:c.1033A>G	XP_006711361.1:p.Thr345Ala
XM_006711299.2:c.1033A>G	XP_006711362.1:p.Thr345Ala
XM_005245139.2:c.843A>G	XP_005245196.1:p.Pro281=
XM_005245140.3:c.843A>G	XP_005245197.1:p.Pro281=
XM_006711298.2:c.1033A>G	XP_006711361.1:p.Thr345Ala
XM_006711299.4:c.1033A>G	XP_006711362.1:p.Thr345Ala
XM_017001199.2:c.1033A>G	XP_016856688.1:p.Thr345Ala
XM_017001200.2:c.985A>G	XP_016856689.1:p.Thr329Ala
XM_017001201.2:c.843A>G	XP_016856690.1:p.Pro281=
NM_000565.4:c.985A>G MANE Select	NP_000556.1:p.Thr329Ala
NM_181359.3:c.985A>G	NP_852004.1:p.Thr329Ala
NM_001382769.1:c.985A>G	NP_001369698.1:p.Thr329Ala
NM_001382770.1:c.1078A>G	NP_001369699.1:p.Thr360Ala
NM_001382771.1:c.1033A>G	NP_001369700.1:p.Thr345Ala
NM_001382772.1:c.979A>G	NP_001369701.1:p.Thr327Ala
NM_001382773.1:c.1033A>G	NP_001369702.1:p.Thr345Ala
NM_001382774.1:c.625A>G	NP_001369703.1:p.Thr209Ala