Canonical Allele Identifier: CA366971862

Gene: IL6 STEAP1B IL6-AS1

Linked Data

• dbSNP Id: rs1360685977
• gnomAD v2: 7-22767162-C-T
• gnomAD v4: 7-22727543-C-T
• MyVariant Identifiers: chr7:g.22767162C>T (hg19) ; chr7:g.22727543C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22727543C>T , CM000669.2:g.22727543C>T	GRCh38
NC_000007.13:g.22767162C>T , CM000669.1:g.22767162C>T	GRCh37
NC_000007.12:g.22733687C>T	NCBI36
NG_011640.1:g.5397C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.367C>T (IL6)
ENST00000258743.10:c.119C>T (IL6) MANE Select	ENSP00000258743.5:p.Ala40Val
ENST00000650428.1:n.46+25G>A (STEAP1B)
ENST00000258743.9:c.119C>T (IL6)	ENSP00000258743.5:p.Ala40Val
ENST00000401630.7:c.50C>T (IL6)	ENSP00000384928.3:p.Ala17Val
ENST00000401651.5:c.-19+262C>T (IL6)	ENSP00000385718.1:n.-19+262C>T
ENST00000404625.5:c.119C>T (IL6)	ENSP00000385675.1:p.Ala40Val
ENST00000406575.1:c.119C>T (IL6)	ENSP00000385227.1:p.Ala40Val
ENST00000407492.5:c.-19+262C>T (IL6)	ENSP00000385043.1:n.-19+262C>T
ENST00000426291.5:c.119C>T (IL6)	ENSP00000405150.1:p.Ala40Val
ENST00000485300.1:n.344C>T (IL6)
NM_000600.3:c.119C>T (IL6)	NP_000591.1:p.Ala40Val
NR_131935.1:n.53+25G>A (IL6-AS1)
XM_005249745.3:c.281C>T (IL6)	XP_005249802.1:p.Ala94Val
XM_011515390.1:c.119C>T (IL6)	XP_011513692.1:p.Ala40Val
XM_011515391.1:c.-19+262C>T (IL6)	XP_011513693.1:n.-19+262C>T
NM_000600.4:c.119C>T (IL6)	NP_000591.1:p.Ala40Val
NM_001318095.1:c.-19+262C>T (IL6)	NP_001305024.1:n.-19+262C>T
XM_005249745.5:c.281C>T (IL6)	XP_005249802.1:p.Ala94Val
XM_011515390.2:c.119C>T (IL6)	XP_011513692.1:p.Ala40Val
NM_000600.5:c.119C>T (IL6) MANE Select	NP_000591.1:p.Ala40Val
NM_001318095.2:c.-19+262C>T (IL6)	NP_001305024.1:n.-19+262C>T
NM_001371096.1:c.50C>T (IL6)	NP_001358025.1:p.Ala17Val