Canonical Allele Identifier: CA155238507

Gene: IL6 STEAP1B IL6-AS1

Linked Data

• dbSNP Id: rs958965295
• gnomAD v2: 7-22766891-T-G
• gnomAD v4: 7-22727272-T-G
• COSMIC: COSM6177332 ; COSM6177333
• MyVariant Identifiers: chr7:g.22766891T>G (hg19) ; chr7:g.22727272T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22727272T>G , CM000669.2:g.22727272T>G	GRCh38
NC_000007.13:g.22766891T>G , CM000669.1:g.22766891T>G	GRCh37
NC_000007.12:g.22733416T>G	NCBI36
NG_011640.1:g.5126T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.96T>G (IL6)
ENST00000258743.10:c.10T>G (IL6) MANE Select	ENSP00000258743.5:p.Phe4Val
ENST00000650428.1:n.46+296A>C (STEAP1B)
ENST00000258743.9:c.10T>G (IL6)	ENSP00000258743.5:p.Phe4Val
ENST00000401630.7:c.10T>G (IL6)	ENSP00000384928.3:p.Phe4Val
ENST00000401651.5:c.-28T>G (IL6)	ENSP00000385718.1:n.-28T>G
ENST00000404625.5:c.10T>G (IL6)	ENSP00000385675.1:p.Phe4Val
ENST00000406575.1:c.10T>G (IL6)	ENSP00000385227.1:p.Phe4Val
ENST00000407492.5:c.-28T>G (IL6)	ENSP00000385043.1:n.-28T>G
ENST00000426291.5:c.10T>G (IL6)	ENSP00000405150.1:p.Phe4Val
ENST00000485300.1:n.73T>G (IL6)
NM_000600.3:c.10T>G (IL6)	NP_000591.1:p.Phe4Val
NR_131935.1:n.53+296A>C (IL6-AS1)
XM_005249745.3:c.10T>G (IL6)	XP_005249802.1:p.Phe4Val
XM_011515390.1:c.10T>G (IL6)	XP_011513692.1:p.Phe4Val
XM_011515391.1:c.-28T>G (IL6)	XP_011513693.1:n.-28T>G
NM_000600.4:c.10T>G (IL6)	NP_000591.1:p.Phe4Val
NM_001318095.1:c.-28T>G (IL6)	NP_001305024.1:n.-28T>G
XM_005249745.5:c.10T>G (IL6)	XP_005249802.1:p.Phe4Val
XM_011515390.2:c.10T>G (IL6)	XP_011513692.1:p.Phe4Val
NM_000600.5:c.10T>G (IL6) MANE Select	NP_000591.1:p.Phe4Val
NM_001318095.2:c.-28T>G (IL6)	NP_001305024.1:n.-28T>G
NM_001371096.1:c.10T>G (IL6)	NP_001358025.1:p.Phe4Val