Canonical Allele Identifier: CA155238370

Gene: STEAP1B IL6 IL6-AS1

Linked Data

• dbSNP Id: rs1002148681
• gnomAD v4: 7-22727152-T-C
• MyVariant Identifiers: chr7:g.22766771T>C (hg19) ; chr7:g.22727152T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22727152T>C , CM000669.2:g.22727152T>C	GRCh38
NC_000007.13:g.22766771T>C , CM000669.1:g.22766771T>C	GRCh37
NC_000007.12:g.22733296T>C	NCBI36
NG_011640.1:g.5006T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650428.1:n.46+416A>G (STEAP1B)
ENST00000258743.9:c.-111T>C (IL6)	ENSP00000258743.5:n.-111T>C
ENST00000401651.5:c.-148T>C (IL6)	ENSP00000385718.1:n.-148T>C
ENST00000404625.5:c.-84-27T>C (IL6)	ENSP00000385675.1:n.-84-27T>C
ENST00000426291.5:c.-111T>C (IL6)	ENSP00000405150.1:n.-111T>C
NM_000600.3:c.-111T>C (IL6)	NP_000591.1:n.-111T>C
NR_131935.1:n.53+416A>G (IL6-AS1)
XM_005249745.3:c.-111T>C (IL6)	XP_005249802.1:n.-111T>C
XM_011515390.1:c.-84-27T>C (IL6)	XP_011513692.1:n.-84-27T>C
NM_000600.4:c.-111T>C (IL6)	NP_000591.1:n.-111T>C
NM_001318095.1:c.-148T>C (IL6)	NP_001305024.1:n.-148T>C
XM_011515390.2:c.-84-27T>C (IL6)	XP_011513692.1:n.-84-27T>C