Canonical Allele Identifier: CA2739947754

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727302G>C , CM000669.2:g.22727302G>C GRCh38
NC_000007.13:g.22766921G>C , CM000669.1:g.22766921G>C GRCh37
NC_000007.12:g.22733446G>C NCBI36
NG_011640.1:g.5156G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000464710.2:n.126G>C (IL6)
ENST00000258743.10:c.19+21G>C (IL6) MANE Select ENSP00000258743.5:n.19+21G>C
ENST00000650428.1:n.46+266C>G (STEAP1B)
ENST00000258743.9:c.19+21G>C (IL6) ENSP00000258743.5:n.19+21G>C
ENST00000401630.7:c.19+21G>C (IL6) ENSP00000384928.3:n.19+21G>C
ENST00000401651.5:c.-19+21G>C (IL6) ENSP00000385718.1:n.-19+21G>C
ENST00000404625.5:c.19+21G>C (IL6) ENSP00000385675.1:n.19+21G>C
ENST00000406575.1:c.19+21G>C (IL6) ENSP00000385227.1:n.19+21G>C
ENST00000407492.5:c.-19+21G>C (IL6) ENSP00000385043.1:n.-19+21G>C
ENST00000426291.5:c.19+21G>C (IL6) ENSP00000405150.1:n.19+21G>C
ENST00000485300.1:n.103G>C (IL6)
NM_000600.3:c.19+21G>C (IL6) NP_000591.1:n.19+21G>C
NR_131935.1:n.53+266C>G (IL6-AS1)
XM_005249745.3:c.40G>C (IL6) XP_005249802.1:p.Ala14Pro
XM_011515390.1:c.19+21G>C (IL6) XP_011513692.1:n.19+21G>C
XM_011515391.1:c.-19+21G>C (IL6) XP_011513693.1:n.-19+21G>C
NM_000600.4:c.19+21G>C (IL6) NP_000591.1:n.19+21G>C
NM_001318095.1:c.-19+21G>C (IL6) NP_001305024.1:n.-19+21G>C
XM_005249745.5:c.40G>C (IL6) XP_005249802.1:p.Ala14Pro
XM_011515390.2:c.19+21G>C (IL6) XP_011513692.1:n.19+21G>C
NM_000600.5:c.19+21G>C (IL6) MANE Select NP_000591.1:n.19+21G>C
NM_001318095.2:c.-19+21G>C (IL6) NP_001305024.1:n.-19+21G>C
NM_001371096.1:c.19+21G>C (IL6) NP_001358025.1:n.19+21G>C