Canonical Allele Identifier: CA420975947

Gene: IL6R

Linked Data

• dbSNP Id: rs1691496804
• MyVariant Identifiers: chr1:g.154437712C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465236C>T , CM000663.2:g.154465236C>T	GRCh38
NC_000001.10:g.154437712C>T , CM000663.1:g.154437712C>T	GRCh37
NC_000001.9:g.152704336C>T	NCBI36
NG_012087.1:g.65044C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1263C>T MANE Select	ENSP00000357470.3:p.Thr421=
ENST00000344086.8:c.*71C>T	ENSP00000340589.4:n.*71C>T
ENST00000368485.7:c.1263C>T	ENSP00000357470.3:p.Thr421=
ENST00000502679.1:n.576C>T
ENST00000507256.1:n.461C>T
NM_000565.3:c.1263C>T	NP_000556.1:p.Thr421=
NM_181359.2:c.*71C>T	NP_852004.1:n.*71C>T
XM_005245139.1:c.1027C>T	XP_005245196.1:p.Pro343Ser
XM_005245140.1:c.*104C>T	XP_005245197.1:n.*104C>T
XM_006711298.1:c.1311C>T	XP_006711361.1:p.Thr437=
XM_006711299.2:c.*71C>T	XP_006711362.1:n.*71C>T
XM_005245139.2:c.1027C>T	XP_005245196.1:p.Pro343Ser
XM_005245140.3:c.*104C>T	XP_005245197.1:n.*104C>T
XM_006711298.2:c.1311C>T	XP_006711361.1:p.Thr437=
XM_006711299.4:c.*71C>T	XP_006711362.1:n.*71C>T
XM_017001199.2:c.1410C>T	XP_016856688.1:p.Thr470=
XM_017001200.2:c.1362C>T	XP_016856689.1:p.Thr454=
XM_017001201.2:c.*104C>T	XP_016856690.1:n.*104C>T
NM_000565.4:c.1263C>T MANE Select	NP_000556.1:p.Thr421=
NM_181359.3:c.*71C>T	NP_852004.1:n.*71C>T
NM_001382769.1:c.1362C>T	NP_001369698.1:p.Thr454=
NM_001382770.1:c.1356C>T	NP_001369699.1:p.Thr452=
NM_001382771.1:c.1311C>T	NP_001369700.1:p.Thr437=
NM_001382772.1:c.1257C>T	NP_001369701.1:p.Thr419=
NM_001382773.1:c.*71C>T	NP_001369702.1:n.*71C>T
NM_001382774.1:c.903C>T	NP_001369703.1:p.Thr301=