Canonical Allele Identifier: CA366971788

Gene: IL6 STEAP1B IL6-AS1

Linked Data

• gnomAD v4: 7-22727510-C-G
• MyVariant Identifiers: chr7:g.22767129C>G (hg19) ; chr7:g.22727510C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22727510C>G , CM000669.2:g.22727510C>G	GRCh38
NC_000007.13:g.22767129C>G , CM000669.1:g.22767129C>G	GRCh37
NC_000007.12:g.22733654C>G	NCBI36
NG_011640.1:g.5364C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.334C>G (IL6)
ENST00000258743.10:c.86C>G (IL6) MANE Select	ENSP00000258743.5:p.Pro29Arg
ENST00000650428.1:n.46+58G>C (STEAP1B)
ENST00000258743.9:c.86C>G (IL6)	ENSP00000258743.5:p.Pro29Arg
ENST00000401630.7:c.20-3C>G (IL6)	ENSP00000384928.3:n.20-3C>G
ENST00000401651.5:c.-19+229C>G (IL6)	ENSP00000385718.1:n.-19+229C>G
ENST00000404625.5:c.86C>G (IL6)	ENSP00000385675.1:p.Pro29Arg
ENST00000406575.1:c.86C>G (IL6)	ENSP00000385227.1:p.Pro29Arg
ENST00000407492.5:c.-19+229C>G (IL6)	ENSP00000385043.1:n.-19+229C>G
ENST00000426291.5:c.86C>G (IL6)	ENSP00000405150.1:p.Pro29Arg
ENST00000485300.1:n.311C>G (IL6)
NM_000600.3:c.86C>G (IL6)	NP_000591.1:p.Pro29Arg
NR_131935.1:n.53+58G>C (IL6-AS1)
XM_005249745.3:c.248C>G (IL6)	XP_005249802.1:p.Pro83Arg
XM_011515390.1:c.86C>G (IL6)	XP_011513692.1:p.Pro29Arg
XM_011515391.1:c.-19+229C>G (IL6)	XP_011513693.1:n.-19+229C>G
NM_000600.4:c.86C>G (IL6)	NP_000591.1:p.Pro29Arg
NM_001318095.1:c.-19+229C>G (IL6)	NP_001305024.1:n.-19+229C>G
XM_005249745.5:c.248C>G (IL6)	XP_005249802.1:p.Pro83Arg
XM_011515390.2:c.86C>G (IL6)	XP_011513692.1:p.Pro29Arg
NM_000600.5:c.86C>G (IL6) MANE Select	NP_000591.1:p.Pro29Arg
NM_001318095.2:c.-19+229C>G (IL6)	NP_001305024.1:n.-19+229C>G
NM_001371096.1:c.20-3C>G (IL6)	NP_001358025.1:n.20-3C>G