Canonical Allele Identifier: CA2509465391

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727178G>A , CM000669.2:g.22727178G>A GRCh38
NC_000007.13:g.22766797G>A , CM000669.1:g.22766797G>A GRCh37
NC_000007.12:g.22733322G>A NCBI36
NG_011640.1:g.5032G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000464710.2:n.2G>A (IL6)
ENST00000650428.1:n.46+390C>T (STEAP1B)
ENST00000258743.9:c.-85G>A (IL6) ENSP00000258743.5:n.-85G>A
ENST00000401651.5:c.-122G>A (IL6) ENSP00000385718.1:n.-122G>A
ENST00000404625.5:c.-84-1G>A (IL6) ENSP00000385675.1:n.-84-1G>A
ENST00000426291.5:c.-85G>A (IL6) ENSP00000405150.1:n.-85G>A
NM_000600.3:c.-85G>A (IL6) NP_000591.1:n.-85G>A
NR_131935.1:n.53+390C>T (IL6-AS1)
XM_005249745.3:c.-85G>A (IL6) XP_005249802.1:n.-85G>A
XM_011515390.1:c.-84-1G>A (IL6) XP_011513692.1:n.-84-1G>A
XM_011515391.1:c.-122G>A (IL6) XP_011513693.1:n.-122G>A
NM_000600.4:c.-85G>A (IL6) NP_000591.1:n.-85G>A
NM_001318095.1:c.-122G>A (IL6) NP_001305024.1:n.-122G>A
XM_005249745.5:c.-85G>A (IL6) XP_005249802.1:n.-85G>A
XM_011515390.2:c.-84-1G>A (IL6) XP_011513692.1:n.-84-1G>A