Canonical Allele Identifier: CA1129298

Gene: IL6R

Linked Data

• dbSNP Id: rs759335112
• ExAC: 1:154437565 G / A
• gnomAD v2: 1-154437565-G-A
• gnomAD v4: 1-154465089-G-A
• MyVariant Identifiers: chr1:g.154437565G>A (hg19) ; chr1:g.154465089G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465089G>A , CM000663.2:g.154465089G>A	GRCh38
NC_000001.10:g.154437565G>A , CM000663.1:g.154437565G>A	GRCh37
NC_000001.9:g.152704189G>A	NCBI36
NG_012087.1:g.64897G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1161-45G>A MANE Select	ENSP00000357470.3:n.1161-45G>A
ENST00000344086.8:c.1067-45G>A	ENSP00000340589.4:n.1067-45G>A
ENST00000368485.7:c.1161-45G>A	ENSP00000357470.3:n.1161-45G>A
ENST00000502679.1:n.474-45G>A
ENST00000507256.1:n.359-45G>A
NM_000565.3:c.1161-45G>A	NP_000556.1:n.1161-45G>A
NM_181359.2:c.1067-45G>A	NP_852004.1:n.1067-45G>A
XM_005245139.1:c.925-45G>A	XP_005245196.1:n.925-45G>A
XM_005245140.1:c.*2-45G>A	XP_005245197.1:n.*2-45G>A
XM_006711298.1:c.1209-45G>A	XP_006711361.1:n.1209-45G>A
XM_006711299.2:c.1115-45G>A	XP_006711362.1:n.1115-45G>A
XM_005245139.2:c.925-45G>A	XP_005245196.1:n.925-45G>A
XM_005245140.3:c.*2-45G>A	XP_005245197.1:n.*2-45G>A
XM_006711298.2:c.1209-45G>A	XP_006711361.1:n.1209-45G>A
XM_006711299.4:c.1115-45G>A	XP_006711362.1:n.1115-45G>A
XM_017001199.2:c.1308-45G>A	XP_016856688.1:n.1308-45G>A
XM_017001200.2:c.1260-45G>A	XP_016856689.1:n.1260-45G>A
XM_017001201.2:c.*2-45G>A	XP_016856690.1:n.*2-45G>A
NM_000565.4:c.1161-45G>A MANE Select	NP_000556.1:n.1161-45G>A
NM_181359.3:c.1067-45G>A	NP_852004.1:n.1067-45G>A
NM_001382769.1:c.1260-45G>A	NP_001369698.1:n.1260-45G>A
NM_001382770.1:c.1254-45G>A	NP_001369699.1:n.1254-45G>A
NM_001382771.1:c.1209-45G>A	NP_001369700.1:n.1209-45G>A
NM_001382772.1:c.1155-45G>A	NP_001369701.1:n.1155-45G>A
NM_001382773.1:c.1115-45G>A	NP_001369702.1:n.1115-45G>A
NM_001382774.1:c.801-45G>A	NP_001369703.1:n.801-45G>A