Canonical Allele Identifier: CA155238419

Gene: IL6 STEAP1B IL6-AS1

Linked Data

• dbSNP Id: rs199671830
• gnomAD v4: 7-22727207-C-T
• MyVariant Identifiers: chr7:g.22766826C>T (hg19) ; chr7:g.22727207C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22727207C>T , CM000669.2:g.22727207C>T	GRCh38
NC_000007.13:g.22766826C>T , CM000669.1:g.22766826C>T	GRCh37
NC_000007.12:g.22733351C>T	NCBI36
NG_011640.1:g.5061C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.31C>T (IL6)
ENST00000258743.10:c.-56C>T (IL6) MANE Select	ENSP00000258743.5:n.-56C>T
ENST00000650428.1:n.46+361G>A (STEAP1B)
ENST00000258743.9:c.-56C>T (IL6)	ENSP00000258743.5:n.-56C>T
ENST00000401651.5:c.-93C>T (IL6)	ENSP00000385718.1:n.-93C>T
ENST00000404625.5:c.-56C>T (IL6)	ENSP00000385675.1:n.-56C>T
ENST00000426291.5:c.-56C>T (IL6)	ENSP00000405150.1:n.-56C>T
ENST00000485300.1:n.8C>T (IL6)
NM_000600.3:c.-56C>T (IL6)	NP_000591.1:n.-56C>T
NR_131935.1:n.53+361G>A (IL6-AS1)
XM_005249745.3:c.-56C>T (IL6)	XP_005249802.1:n.-56C>T
XM_011515390.1:c.-56C>T (IL6)	XP_011513692.1:n.-56C>T
XM_011515391.1:c.-93C>T (IL6)	XP_011513693.1:n.-93C>T
NM_000600.4:c.-56C>T (IL6)	NP_000591.1:n.-56C>T
NM_001318095.1:c.-93C>T (IL6)	NP_001305024.1:n.-93C>T
XM_005249745.5:c.-56C>T (IL6)	XP_005249802.1:n.-56C>T
XM_011515390.2:c.-56C>T (IL6)	XP_011513692.1:n.-56C>T
NM_000600.5:c.-56C>T (IL6) MANE Select	NP_000591.1:n.-56C>T
NM_001318095.2:c.-93C>T (IL6)	NP_001305024.1:n.-93C>T
NM_001371096.1:c.-56C>T (IL6)	NP_001358025.1:n.-56C>T