Canonical Allele Identifier: CA1007937895

Gene: IL6R

Linked Data

• ClinVar Variation Id: 2991734
• ClinVar RCV Id: RCV003852797
• dbSNP Id: rs769292401
• gnomAD v3: 1-154454470-A-T
• gnomAD v4: 1-154454470-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154454470A>T , CM000663.2:g.154454470A>T	GRCh38
NC_000001.10:g.154426946A>T , CM000663.1:g.154426946A>T	GRCh37
NC_000001.9:g.152693570A>T	NCBI36
NG_012087.1:g.54278A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1067-18A>T MANE Select	ENSP00000357470.3:n.1067-18A>T
ENST00000344086.8:c.1066+4490A>T	ENSP00000340589.4:n.1066+4490A>T
ENST00000368485.7:c.1067-18A>T	ENSP00000357470.3:n.1067-18A>T
ENST00000502679.1:n.362A>T
ENST00000507256.1:n.265-18A>T
ENST00000515190.1:c.475-18A>T
NM_000565.3:c.1067-18A>T	NP_000556.1:n.1067-18A>T
NM_181359.2:c.1066+4490A>T	NP_852004.1:n.1066+4490A>T
XM_005245139.1:c.924+4490A>T	XP_005245196.1:n.924+4490A>T
XM_005245140.1:c.925-18A>T	XP_005245197.1:n.925-18A>T
XM_006711298.1:c.1115-18A>T	XP_006711361.1:n.1115-18A>T
XM_006711299.2:c.1114+4490A>T	XP_006711362.1:n.1114+4490A>T
XM_005245139.2:c.924+4490A>T	XP_005245196.1:n.924+4490A>T
XM_005245140.3:c.925-18A>T	XP_005245197.1:n.925-18A>T
XM_006711298.2:c.1115-18A>T	XP_006711361.1:n.1115-18A>T
XM_006711299.4:c.1114+4490A>T	XP_006711362.1:n.1114+4490A>T
XM_017001199.2:c.1214-18A>T	XP_016856688.1:n.1214-18A>T
XM_017001200.2:c.1166-18A>T	XP_016856689.1:n.1166-18A>T
XM_017001201.2:c.1024-18A>T	XP_016856690.1:n.1024-18A>T
NM_000565.4:c.1067-18A>T MANE Select	NP_000556.1:n.1067-18A>T
NM_181359.3:c.1066+4490A>T	NP_852004.1:n.1066+4490A>T
NM_001382769.1:c.1166-18A>T	NP_001369698.1:n.1166-18A>T
NM_001382770.1:c.1160-18A>T	NP_001369699.1:n.1160-18A>T
NM_001382771.1:c.1115-18A>T	NP_001369700.1:n.1115-18A>T
NM_001382772.1:c.1061-18A>T	NP_001369701.1:n.1061-18A>T
NM_001382773.1:c.1114+4490A>T	NP_001369702.1:n.1114+4490A>T
NM_001382774.1:c.707-18A>T	NP_001369703.1:n.707-18A>T