Canonical Allele Identifier: CA4185317

Gene: IL6 STEAP1B IL6-AS1

Linked Data

• dbSNP Id: rs199957016
• ExAC: 7:22767173 A / C
• gnomAD v2: 7-22767173-A-C
• gnomAD v3: 7-22727554-A-C
• gnomAD v4: 7-22727554-A-C
• MyVariant Identifiers: chr7:g.22767173A>C (hg19) ; chr7:g.22727554A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22727554A>C , CM000669.2:g.22727554A>C	GRCh38
NC_000007.13:g.22767173A>C , CM000669.1:g.22767173A>C	GRCh37
NC_000007.12:g.22733698A>C	NCBI36
NG_011640.1:g.5408A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.378A>C (IL6)
ENST00000258743.10:c.130A>C (IL6) MANE Select	ENSP00000258743.5:p.Arg44=
ENST00000650428.1:n.46+14T>G (STEAP1B)
ENST00000258743.9:c.130A>C (IL6)	ENSP00000258743.5:p.Arg44=
ENST00000401630.7:c.61A>C (IL6)	ENSP00000384928.3:p.Arg21=
ENST00000401651.5:c.-19+273A>C (IL6)	ENSP00000385718.1:n.-19+273A>C
ENST00000404625.5:c.130A>C (IL6)	ENSP00000385675.1:p.Arg44=
ENST00000406575.1:c.130A>C (IL6)	ENSP00000385227.1:p.Arg44=
ENST00000407492.5:c.-19+273A>C (IL6)	ENSP00000385043.1:n.-19+273A>C
ENST00000426291.5:c.130A>C (IL6)	ENSP00000405150.1:p.Arg44=
ENST00000485300.1:n.355A>C (IL6)
NM_000600.3:c.130A>C (IL6)	NP_000591.1:p.Arg44=
NR_131935.1:n.53+14T>G (IL6-AS1)
XM_005249745.3:c.292A>C (IL6)	XP_005249802.1:p.Arg98=
XM_011515390.1:c.130A>C (IL6)	XP_011513692.1:p.Arg44=
XM_011515391.1:c.-19+273A>C (IL6)	XP_011513693.1:n.-19+273A>C
NM_000600.4:c.130A>C (IL6)	NP_000591.1:p.Arg44=
NM_001318095.1:c.-19+273A>C (IL6)	NP_001305024.1:n.-19+273A>C
XM_005249745.5:c.292A>C (IL6)	XP_005249802.1:p.Arg98=
XM_011515390.2:c.130A>C (IL6)	XP_011513692.1:p.Arg44=
NM_000600.5:c.130A>C (IL6) MANE Select	NP_000591.1:p.Arg44=
NM_001318095.2:c.-19+273A>C (IL6)	NP_001305024.1:n.-19+273A>C
NM_001371096.1:c.61A>C (IL6)	NP_001358025.1:p.Arg21=