Canonical Allele Identifier: CA15485195

Gene: IL6

Linked Data

• dbSNP Id: rs1474347
• gnomAD v2: 7-22768124-C-A
• gnomAD v3: 7-22728505-C-A
• gnomAD v4: 7-22728505-C-A
• MyVariant Identifiers: chr7:g.22768124C>A (hg19) ; chr7:g.22728505C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22728505C>A , CM000669.2:g.22728505C>A	GRCh38
NC_000007.13:g.22768124C>A , CM000669.1:g.22768124C>A	GRCh37
NC_000007.12:g.22734649C>A	NCBI36
NG_011640.1:g.6359C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000464710.2:n.1329C>A
ENST00000258743.10:c.211-188C>A MANE Select	ENSP00000258743.5:n.211-188C>A
ENST00000258743.9:c.211-188C>A	ENSP00000258743.5:n.211-188C>A
ENST00000401630.7:c.142-188C>A	ENSP00000384928.3:n.142-188C>A
ENST00000401651.5:c.-18-188C>A	ENSP00000385718.1:n.-18-188C>A
ENST00000404625.5:c.211-188C>A	ENSP00000385675.1:n.211-188C>A
ENST00000406575.1:c.211-188C>A	ENSP00000385227.1:n.211-188C>A
ENST00000407492.5:c.-18-188C>A	ENSP00000385043.1:n.-18-188C>A
ENST00000426291.5:c.211-188C>A	ENSP00000405150.1:n.211-188C>A
ENST00000464710.1:n.6C>A
ENST00000485300.1:n.436-188C>A
NM_000600.3:c.211-188C>A	NP_000591.1:n.211-188C>A
XM_005249745.3:c.373-188C>A	XP_005249802.1:n.373-188C>A
XM_011515390.1:c.211-188C>A	XP_011513692.1:n.211-188C>A
XM_011515391.1:c.-18-188C>A	XP_011513693.1:n.-18-188C>A
NM_000600.4:c.211-188C>A	NP_000591.1:n.211-188C>A
NM_001318095.1:c.-18-188C>A	NP_001305024.1:n.-18-188C>A
XM_005249745.5:c.373-188C>A	XP_005249802.1:n.373-188C>A
XM_011515390.2:c.211-188C>A	XP_011513692.1:n.211-188C>A
NM_000600.5:c.211-188C>A MANE Select	NP_000591.1:n.211-188C>A
NM_001318095.2:c.-18-188C>A	NP_001305024.1:n.-18-188C>A
NM_001371096.1:c.142-188C>A	NP_001358025.1:n.142-188C>A