Canonical Allele Identifier: CA342628414

Gene: IL6R

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1204A>G MANE Select	ENSP00000357470.3:p.Thr402Ala
ENST00000344086.8:c.*12A>G	ENSP00000340589.4:n.*12A>G
ENST00000368485.7:c.1204A>G	ENSP00000357470.3:p.Thr402Ala
ENST00000502679.1:n.517A>G
ENST00000507256.1:n.402A>G
NM_000565.3:c.1204A>G	NP_000556.1:p.Thr402Ala
NM_181359.2:c.*12A>G	NP_852004.1:n.*12A>G
XM_005245139.1:c.968A>G	XP_005245196.1:p.Asp323Gly
XM_005245140.1:c.*45A>G	XP_005245197.1:n.*45A>G
XM_006711298.1:c.1252A>G	XP_006711361.1:p.Thr418Ala
XM_006711299.2:c.*12A>G	XP_006711362.1:n.*12A>G
XM_005245139.2:c.968A>G	XP_005245196.1:p.Asp323Gly
XM_005245140.3:c.*45A>G	XP_005245197.1:n.*45A>G
XM_006711298.2:c.1252A>G	XP_006711361.1:p.Thr418Ala
XM_006711299.4:c.*12A>G	XP_006711362.1:n.*12A>G
XM_017001199.2:c.1351A>G	XP_016856688.1:p.Thr451Ala
XM_017001200.2:c.1303A>G	XP_016856689.1:p.Thr435Ala
XM_017001201.2:c.*45A>G	XP_016856690.1:n.*45A>G
NM_000565.4:c.1204A>G MANE Select	NP_000556.1:p.Thr402Ala
NM_181359.3:c.*12A>G	NP_852004.1:n.*12A>G
NM_001382769.1:c.1303A>G	NP_001369698.1:p.Thr435Ala
NM_001382770.1:c.1297A>G	NP_001369699.1:p.Thr433Ala
NM_001382771.1:c.1252A>G	NP_001369700.1:p.Thr418Ala
NM_001382772.1:c.1198A>G	NP_001369701.1:p.Thr400Ala
NM_001382773.1:c.*12A>G	NP_001369702.1:n.*12A>G
NM_001382774.1:c.844A>G	NP_001369703.1:p.Thr282Ala