Canonical Allele Identifier: CA4185262

Gene: IL6 STEAP1B IL6-AS1

Linked Data

• dbSNP Id: rs765378428
• ExAC: 7:22766911 G / A
• gnomAD v2: 7-22766911-G-A
• gnomAD v4: 7-22727292-G-A
• MyVariant Identifiers: chr7:g.22766911G>A (hg19) ; chr7:g.22727292G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22727292G>A , CM000669.2:g.22727292G>A	GRCh38
NC_000007.13:g.22766911G>A , CM000669.1:g.22766911G>A	GRCh37
NC_000007.12:g.22733436G>A	NCBI36
NG_011640.1:g.5146G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.116G>A (IL6)
ENST00000258743.10:c.19+11G>A (IL6) MANE Select	ENSP00000258743.5:n.19+11G>A
ENST00000650428.1:n.46+276C>T (STEAP1B)
ENST00000258743.9:c.19+11G>A (IL6)	ENSP00000258743.5:n.19+11G>A
ENST00000401630.7:c.19+11G>A (IL6)	ENSP00000384928.3:n.19+11G>A
ENST00000401651.5:c.-19+11G>A (IL6)	ENSP00000385718.1:n.-19+11G>A
ENST00000404625.5:c.19+11G>A (IL6)	ENSP00000385675.1:n.19+11G>A
ENST00000406575.1:c.19+11G>A (IL6)	ENSP00000385227.1:n.19+11G>A
ENST00000407492.5:c.-19+11G>A (IL6)	ENSP00000385043.1:n.-19+11G>A
ENST00000426291.5:c.19+11G>A (IL6)	ENSP00000405150.1:n.19+11G>A
ENST00000485300.1:n.93G>A (IL6)
NM_000600.3:c.19+11G>A (IL6)	NP_000591.1:n.19+11G>A
NR_131935.1:n.53+276C>T (IL6-AS1)
XM_005249745.3:c.30G>A (IL6)	XP_005249802.1:p.Arg10=
XM_011515390.1:c.19+11G>A (IL6)	XP_011513692.1:n.19+11G>A
XM_011515391.1:c.-19+11G>A (IL6)	XP_011513693.1:n.-19+11G>A
NM_000600.4:c.19+11G>A (IL6)	NP_000591.1:n.19+11G>A
NM_001318095.1:c.-19+11G>A (IL6)	NP_001305024.1:n.-19+11G>A
XM_005249745.5:c.30G>A (IL6)	XP_005249802.1:p.Arg10=
XM_011515390.2:c.19+11G>A (IL6)	XP_011513692.1:n.19+11G>A
NM_000600.5:c.19+11G>A (IL6) MANE Select	NP_000591.1:n.19+11G>A
NM_001318095.2:c.-19+11G>A (IL6)	NP_001305024.1:n.-19+11G>A
NM_001371096.1:c.19+11G>A (IL6)	NP_001358025.1:n.19+11G>A