Canonical Allele Identifier: CA4185311

Linked Data

ClinVar Variation Id: 768143
ClinVar RCV Id: RCV000947003
dbSNP Id: rs2069830
gnomAD v2: 7-22767137-C-T
gnomAD v3: 7-22727518-C-T
gnomAD v4: 7-22727518-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727518C>T , CM000669.2:g.22727518C>T GRCh38
NC_000007.13:g.22767137C>T , CM000669.1:g.22767137C>T GRCh37
NC_000007.12:g.22733662C>T NCBI36
NG_011640.1:g.5372C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000464710.2:n.342C>T (IL6)
ENST00000258743.10:c.94C>T (IL6) MANE Select ENSP00000258743.5:p.Pro32Ser
ENST00000650428.1:n.46+50G>A (STEAP1B)
ENST00000258743.9:c.94C>T (IL6) ENSP00000258743.5:p.Pro32Ser
ENST00000401630.7:c.25C>T (IL6) ENSP00000384928.3:p.Pro9Ser
ENST00000401651.5:c.-19+237C>T (IL6) ENSP00000385718.1:n.-19+237C>T
ENST00000404625.5:c.94C>T (IL6) ENSP00000385675.1:p.Pro32Ser
ENST00000406575.1:c.94C>T (IL6) ENSP00000385227.1:p.Pro32Ser
ENST00000407492.5:c.-19+237C>T (IL6) ENSP00000385043.1:n.-19+237C>T
ENST00000426291.5:c.94C>T (IL6) ENSP00000405150.1:p.Pro32Ser
ENST00000485300.1:n.319C>T (IL6)
NM_000600.3:c.94C>T (IL6) NP_000591.1:p.Pro32Ser
NR_131935.1:n.53+50G>A (IL6-AS1)
XM_005249745.3:c.256C>T (IL6) XP_005249802.1:p.Pro86Ser
XM_011515390.1:c.94C>T (IL6) XP_011513692.1:p.Pro32Ser
XM_011515391.1:c.-19+237C>T (IL6) XP_011513693.1:n.-19+237C>T
NM_000600.4:c.94C>T (IL6) NP_000591.1:p.Pro32Ser
NM_001318095.1:c.-19+237C>T (IL6) NP_001305024.1:n.-19+237C>T
XM_005249745.5:c.256C>T (IL6) XP_005249802.1:p.Pro86Ser
XM_011515390.2:c.94C>T (IL6) XP_011513692.1:p.Pro32Ser
NM_000600.5:c.94C>T (IL6) MANE Select NP_000591.1:p.Pro32Ser
NM_001318095.2:c.-19+237C>T (IL6) NP_001305024.1:n.-19+237C>T
NM_001371096.1:c.25C>T (IL6) NP_001358025.1:p.Pro9Ser