Canonical Allele Identifier: CA1694138261

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727181C= , CM000669.2:g.22727181C= GRCh38
NC_000007.13:g.22766800C= , CM000669.1:g.22766800C= GRCh37
NC_000007.12:g.22733325C= NCBI36
NG_011640.1:g.5035C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464710.2:n.5C= (IL6)
ENST00000650428.1:n.46+387G= (STEAP1B)
ENST00000258743.9:c.-82C= (IL6) ENSP00000258743.5:n.-82C=
ENST00000401651.5:c.-119C= (IL6) ENSP00000385718.1:n.-119C=
ENST00000404625.5:c.-82C= (IL6) ENSP00000385675.1:n.-82C=
ENST00000426291.5:c.-82C= (IL6) ENSP00000405150.1:n.-82C=
NM_000600.3:c.-82C= (IL6) NP_000591.1:n.-82C=
NR_131935.1:n.53+387G= (IL6-AS1)
XM_005249745.3:c.-82C= (IL6) XP_005249802.1:n.-82C=
XM_011515390.1:c.-82C= (IL6) XP_011513692.1:n.-82C=
XM_011515391.1:c.-119C= (IL6) XP_011513693.1:n.-119C=
NM_000600.4:c.-82C= (IL6) NP_000591.1:n.-82C=
NM_001318095.1:c.-119C= (IL6) NP_001305024.1:n.-119C=
XM_005249745.5:c.-82C= (IL6) XP_005249802.1:n.-82C=
XM_011515390.2:c.-82C= (IL6) XP_011513692.1:n.-82C=