Canonical Allele Identifier: CA342628415

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437653A>T (hg19) ; chr1:g.154465177A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465177A>T , CM000663.2:g.154465177A>T	GRCh38
NC_000001.10:g.154437653A>T , CM000663.1:g.154437653A>T	GRCh37
NC_000001.9:g.152704277A>T	NCBI36
NG_012087.1:g.64985A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1204A>T MANE Select	ENSP00000357470.3:p.Thr402Ser
ENST00000344086.8:c.*12A>T	ENSP00000340589.4:n.*12A>T
ENST00000368485.7:c.1204A>T	ENSP00000357470.3:p.Thr402Ser
ENST00000502679.1:n.517A>T
ENST00000507256.1:n.402A>T
NM_000565.3:c.1204A>T	NP_000556.1:p.Thr402Ser
NM_181359.2:c.*12A>T	NP_852004.1:n.*12A>T
XM_005245139.1:c.968A>T	XP_005245196.1:p.Asp323Val
XM_005245140.1:c.*45A>T	XP_005245197.1:n.*45A>T
XM_006711298.1:c.1252A>T	XP_006711361.1:p.Thr418Ser
XM_006711299.2:c.*12A>T	XP_006711362.1:n.*12A>T
XM_005245139.2:c.968A>T	XP_005245196.1:p.Asp323Val
XM_005245140.3:c.*45A>T	XP_005245197.1:n.*45A>T
XM_006711298.2:c.1252A>T	XP_006711361.1:p.Thr418Ser
XM_006711299.4:c.*12A>T	XP_006711362.1:n.*12A>T
XM_017001199.2:c.1351A>T	XP_016856688.1:p.Thr451Ser
XM_017001200.2:c.1303A>T	XP_016856689.1:p.Thr435Ser
XM_017001201.2:c.*45A>T	XP_016856690.1:n.*45A>T
NM_000565.4:c.1204A>T MANE Select	NP_000556.1:p.Thr402Ser
NM_181359.3:c.*12A>T	NP_852004.1:n.*12A>T
NM_001382769.1:c.1303A>T	NP_001369698.1:p.Thr435Ser
NM_001382770.1:c.1297A>T	NP_001369699.1:p.Thr433Ser
NM_001382771.1:c.1252A>T	NP_001369700.1:p.Thr418Ser
NM_001382772.1:c.1198A>T	NP_001369701.1:p.Thr400Ser
NM_001382773.1:c.*12A>T	NP_001369702.1:n.*12A>T
NM_001382774.1:c.844A>T	NP_001369703.1:p.Thr282Ser