Canonical Allele Identifier: CA1694138274

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727204T= , CM000669.2:g.22727204T= GRCh38
NC_000007.13:g.22766823T= , CM000669.1:g.22766823T= GRCh37
NC_000007.12:g.22733348T= NCBI36
NG_011640.1:g.5058T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000464710.2:n.28T= (IL6)
ENST00000258743.10:c.-59T= (IL6) MANE Select ENSP00000258743.5:n.-59T=
ENST00000650428.1:n.46+364A= (STEAP1B)
ENST00000258743.9:c.-59T= (IL6) ENSP00000258743.5:n.-59T=
ENST00000401651.5:c.-96T= (IL6) ENSP00000385718.1:n.-96T=
ENST00000404625.5:c.-59T= (IL6) ENSP00000385675.1:n.-59T=
ENST00000426291.5:c.-59T= (IL6) ENSP00000405150.1:n.-59T=
ENST00000485300.1:n.5T= (IL6)
NM_000600.3:c.-59T= (IL6) NP_000591.1:n.-59T=
NR_131935.1:n.53+364A= (IL6-AS1)
XM_005249745.3:c.-59T= (IL6) XP_005249802.1:n.-59T=
XM_011515390.1:c.-59T= (IL6) XP_011513692.1:n.-59T=
XM_011515391.1:c.-96T= (IL6) XP_011513693.1:n.-96T=
NM_000600.4:c.-59T= (IL6) NP_000591.1:n.-59T=
NM_001318095.1:c.-96T= (IL6) NP_001305024.1:n.-96T=
XM_005249745.5:c.-59T= (IL6) XP_005249802.1:n.-59T=
XM_011515390.2:c.-59T= (IL6) XP_011513692.1:n.-59T=
NM_000600.5:c.-59T= (IL6) MANE Select NP_000591.1:n.-59T=
NM_001318095.2:c.-96T= (IL6) NP_001305024.1:n.-96T=
NM_001371096.1:c.-59T= (IL6) NP_001358025.1:n.-59T=