Canonical Allele Identifier: CA155238411

Gene: IL6 STEAP1B IL6-AS1

Linked Data

• dbSNP Id: rs895939328
• gnomAD v3: 7-22727177-A-G
• gnomAD v4: 7-22727177-A-G
• MyVariant Identifiers: chr7:g.22766796A>G (hg19) ; chr7:g.22727177A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22727177A>G , CM000669.2:g.22727177A>G	GRCh38
NC_000007.13:g.22766796A>G , CM000669.1:g.22766796A>G	GRCh37
NC_000007.12:g.22733321A>G	NCBI36
NG_011640.1:g.5031A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464710.2:n.1A>G (IL6)
ENST00000650428.1:n.46+391T>C (STEAP1B)
ENST00000258743.9:c.-86A>G (IL6)	ENSP00000258743.5:n.-86A>G
ENST00000401651.5:c.-123A>G (IL6)	ENSP00000385718.1:n.-123A>G
ENST00000404625.5:c.-84-2A>G (IL6)	ENSP00000385675.1:n.-84-2A>G
ENST00000426291.5:c.-86A>G (IL6)	ENSP00000405150.1:n.-86A>G
NM_000600.3:c.-86A>G (IL6)	NP_000591.1:n.-86A>G
NR_131935.1:n.53+391T>C (IL6-AS1)
XM_005249745.3:c.-86A>G (IL6)	XP_005249802.1:n.-86A>G
XM_011515390.1:c.-84-2A>G (IL6)	XP_011513692.1:n.-84-2A>G
XM_011515391.1:c.-123A>G (IL6)	XP_011513693.1:n.-123A>G
NM_000600.4:c.-86A>G (IL6)	NP_000591.1:n.-86A>G
NM_001318095.1:c.-123A>G (IL6)	NP_001305024.1:n.-123A>G
XM_005249745.5:c.-86A>G (IL6)	XP_005249802.1:n.-86A>G
XM_011515390.2:c.-84-2A>G (IL6)	XP_011513692.1:n.-84-2A>G