Canonical Allele Identifier: CA342621601

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154420603T>A (hg19) ; chr1:g.154448127T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154448127T>A , CM000663.2:g.154448127T>A	GRCh38
NC_000001.10:g.154420603T>A , CM000663.1:g.154420603T>A	GRCh37
NC_000001.9:g.152687227T>A	NCBI36
NG_012087.1:g.47935T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368485.8:c.952T>A MANE Select	ENSP00000357470.3:p.Ser318Thr
ENST00000344086.8:c.952T>A	ENSP00000340589.4:p.Ser318Thr
ENST00000368485.7:c.952T>A	ENSP00000357470.3:p.Ser318Thr
ENST00000476006.5:c.768T>A
ENST00000507256.1:n.150T>A
ENST00000515190.1:c.360T>A
NM_000565.3:c.952T>A	NP_000556.1:p.Ser318Thr
NM_181359.2:c.952T>A	NP_852004.1:p.Ser318Thr
XM_005245139.1:c.810T>A	XP_005245196.1:p.Asn270Lys
XM_005245140.1:c.810T>A	XP_005245197.1:p.Asn270Lys
XM_006711298.1:c.1000T>A	XP_006711361.1:p.Ser334Thr
XM_006711299.2:c.1000T>A	XP_006711362.1:p.Ser334Thr
XM_005245139.2:c.810T>A	XP_005245196.1:p.Asn270Lys
XM_005245140.3:c.810T>A	XP_005245197.1:p.Asn270Lys
XM_006711298.2:c.1000T>A	XP_006711361.1:p.Ser334Thr
XM_006711299.4:c.1000T>A	XP_006711362.1:p.Ser334Thr
XM_017001199.2:c.1000T>A	XP_016856688.1:p.Ser334Thr
XM_017001200.2:c.952T>A	XP_016856689.1:p.Ser318Thr
XM_017001201.2:c.810T>A	XP_016856690.1:p.Asn270Lys
NM_000565.4:c.952T>A MANE Select	NP_000556.1:p.Ser318Thr
NM_181359.3:c.952T>A	NP_852004.1:p.Ser318Thr
NM_001382769.1:c.952T>A	NP_001369698.1:p.Ser318Thr
NM_001382770.1:c.1045T>A	NP_001369699.1:p.Ser349Thr
NM_001382771.1:c.1000T>A	NP_001369700.1:p.Ser334Thr
NM_001382772.1:c.946T>A	NP_001369701.1:p.Ser316Thr
NM_001382773.1:c.1000T>A	NP_001369702.1:p.Ser334Thr
NM_001382774.1:c.592T>A	NP_001369703.1:p.Ser198Thr