Canonical Allele Identifier: CA2682013420

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727192del , CM000669.2:g.22727192del GRCh38
NC_000007.13:g.22766811del , CM000669.1:g.22766811del GRCh37
NC_000007.12:g.22733336del NCBI36
NG_011640.1:g.5046del

Transcript Alleles

HGVS Amino-acid Change
ENST00000464710.2:n.16del (IL6)
ENST00000650428.1:n.46+376del (STEAP1B)
ENST00000258743.9:c.-71del (IL6) ENSP00000258743.5:n.-71del
ENST00000401651.5:c.-108del (IL6) ENSP00000385718.1:n.-108del
ENST00000404625.5:c.-71del (IL6) ENSP00000385675.1:n.-71del
ENST00000426291.5:c.-71del (IL6) ENSP00000405150.1:n.-71del
NM_000600.3:c.-71del (IL6) NP_000591.1:n.-71del
NR_131935.1:n.53+376del (IL6-AS1)
XM_005249745.3:c.-71del (IL6) XP_005249802.1:n.-71del
XM_011515390.1:c.-71del (IL6) XP_011513692.1:n.-71del
XM_011515391.1:c.-108del (IL6) XP_011513693.1:n.-108del
NM_000600.4:c.-71del (IL6) NP_000591.1:n.-71del
NM_001318095.1:c.-108del (IL6) NP_001305024.1:n.-108del
XM_005249745.5:c.-71del (IL6) XP_005249802.1:n.-71del
XM_011515390.2:c.-71del (IL6) XP_011513692.1:n.-71del