Canonical Allele Identifier: CA342628812

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437834C>G (hg19) ; chr1:g.154465358C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465358C>G , CM000663.2:g.154465358C>G	GRCh38
NC_000001.10:g.154437834C>G , CM000663.1:g.154437834C>G	GRCh37
NC_000001.9:g.152704458C>G	NCBI36
NG_012087.1:g.65166C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1385C>G MANE Select	ENSP00000357470.3:p.Thr462Arg
ENST00000344086.8:c.*193C>G	ENSP00000340589.4:n.*193C>G
ENST00000368485.7:c.1385C>G	ENSP00000357470.3:p.Thr462Arg
NM_000565.3:c.1385C>G	NP_000556.1:p.Thr462Arg
NM_181359.2:c.*193C>G	NP_852004.1:n.*193C>G
XM_005245139.1:c.*66C>G	XP_005245196.1:n.*66C>G
XM_005245140.1:c.*226C>G	XP_005245197.1:n.*226C>G
XM_006711298.1:c.1433C>G	XP_006711361.1:p.Thr478Arg
XM_005245139.2:c.*66C>G	XP_005245196.1:n.*66C>G
XM_005245140.3:c.*226C>G	XP_005245197.1:n.*226C>G
XM_006711298.2:c.1433C>G	XP_006711361.1:p.Thr478Arg
XM_017001199.2:c.1532C>G	XP_016856688.1:p.Thr511Arg
XM_017001200.2:c.1484C>G	XP_016856689.1:p.Thr495Arg
XM_017001201.2:c.*226C>G	XP_016856690.1:n.*226C>G
NM_000565.4:c.1385C>G MANE Select	NP_000556.1:p.Thr462Arg
NM_181359.3:c.*193C>G	NP_852004.1:n.*193C>G
NM_001382769.1:c.1484C>G	NP_001369698.1:p.Thr495Arg
NM_001382770.1:c.1478C>G	NP_001369699.1:p.Thr493Arg
NM_001382771.1:c.1433C>G	NP_001369700.1:p.Thr478Arg
NM_001382772.1:c.1379C>G	NP_001369701.1:p.Thr460Arg
NM_001382773.1:c.*193C>G	NP_001369702.1:n.*193C>G
NM_001382774.1:c.1025C>G	NP_001369703.1:p.Thr342Arg