Canonical Allele Identifier: CA526405876

Gene: IL6R

Linked Data

• dbSNP Id: rs1464852218
• gnomAD v2: 1-154426960-C-T
• gnomAD v3: 1-154454484-C-T
• gnomAD v4: 1-154454484-C-T
• MyVariant Identifiers: chr1:g.154426960C>T (hg19) ; chr1:g.154454484C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154454484C>T , CM000663.2:g.154454484C>T	GRCh38
NC_000001.10:g.154426960C>T , CM000663.1:g.154426960C>T	GRCh37
NC_000001.9:g.152693584C>T	NCBI36
NG_012087.1:g.54292C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1067-4C>T MANE Select	ENSP00000357470.3:n.1067-4C>T
ENST00000344086.8:c.1066+4504C>T	ENSP00000340589.4:n.1066+4504C>T
ENST00000368485.7:c.1067-4C>T	ENSP00000357470.3:n.1067-4C>T
ENST00000502679.1:n.376C>T
ENST00000507256.1:n.265-4C>T
ENST00000515190.1:c.475-4C>T
NM_000565.3:c.1067-4C>T	NP_000556.1:n.1067-4C>T
NM_181359.2:c.1066+4504C>T	NP_852004.1:n.1066+4504C>T
XM_005245139.1:c.924+4504C>T	XP_005245196.1:n.924+4504C>T
XM_005245140.1:c.925-4C>T	XP_005245197.1:n.925-4C>T
XM_006711298.1:c.1115-4C>T	XP_006711361.1:n.1115-4C>T
XM_006711299.2:c.1114+4504C>T	XP_006711362.1:n.1114+4504C>T
XM_005245139.2:c.924+4504C>T	XP_005245196.1:n.924+4504C>T
XM_005245140.3:c.925-4C>T	XP_005245197.1:n.925-4C>T
XM_006711298.2:c.1115-4C>T	XP_006711361.1:n.1115-4C>T
XM_006711299.4:c.1114+4504C>T	XP_006711362.1:n.1114+4504C>T
XM_017001199.2:c.1214-4C>T	XP_016856688.1:n.1214-4C>T
XM_017001200.2:c.1166-4C>T	XP_016856689.1:n.1166-4C>T
XM_017001201.2:c.1024-4C>T	XP_016856690.1:n.1024-4C>T
NM_000565.4:c.1067-4C>T MANE Select	NP_000556.1:n.1067-4C>T
NM_181359.3:c.1066+4504C>T	NP_852004.1:n.1066+4504C>T
NM_001382769.1:c.1166-4C>T	NP_001369698.1:n.1166-4C>T
NM_001382770.1:c.1160-4C>T	NP_001369699.1:n.1160-4C>T
NM_001382771.1:c.1115-4C>T	NP_001369700.1:n.1115-4C>T
NM_001382772.1:c.1061-4C>T	NP_001369701.1:n.1061-4C>T
NM_001382773.1:c.1114+4504C>T	NP_001369702.1:n.1114+4504C>T
NM_001382774.1:c.707-4C>T	NP_001369703.1:n.707-4C>T