Canonical Allele Identifier: CA2578845415

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727478_22727480del , CM000669.2:g.22727478_22727480del GRCh38
NC_000007.13:g.22767097_22767099del , CM000669.1:g.22767097_22767099del GRCh37
NC_000007.12:g.22733622_22733624del NCBI36
NG_011640.1:g.5332_5334del

Transcript Alleles

HGVS Amino-acid Change
ENST00000464710.2:n.302_304del (IL6)
ENST00000258743.10:c.54_56del (IL6) MANE Select ENSP00000258743.5:p.Leu19del
ENST00000650428.1:n.46+91_46+93del (STEAP1B)
ENST00000258743.9:c.54_56del (IL6) ENSP00000258743.5:p.Leu19del
ENST00000401630.7:c.20-35_20-33del (IL6) ENSP00000384928.3:n.20-35_20-33del
ENST00000401651.5:c.-19+197_-19+199del (IL6) ENSP00000385718.1:n.-19+197_-19+199del
ENST00000404625.5:c.54_56del (IL6) ENSP00000385675.1:p.Leu19del
ENST00000406575.1:c.54_56del (IL6) ENSP00000385227.1:p.Leu19del
ENST00000407492.5:c.-19+197_-19+199del (IL6) ENSP00000385043.1:n.-19+197_-19+199del
ENST00000426291.5:c.54_56del (IL6) ENSP00000405150.1:p.Leu19del
ENST00000485300.1:n.279_281del (IL6)
NM_000600.3:c.54_56del (IL6) NP_000591.1:p.Leu19del
NR_131935.1:n.53+91_53+93del (IL6-AS1)
XM_005249745.3:c.216_218del (IL6) XP_005249802.1:p.Leu73del
XM_011515390.1:c.54_56del (IL6) XP_011513692.1:p.Leu19del
XM_011515391.1:c.-19+197_-19+199del (IL6) XP_011513693.1:n.-19+197_-19+199del
NM_000600.4:c.54_56del (IL6) NP_000591.1:p.Leu19del
NM_001318095.1:c.-19+197_-19+199del (IL6) NP_001305024.1:n.-19+197_-19+199del
XM_005249745.5:c.216_218del (IL6) XP_005249802.1:p.Leu73del
XM_011515390.2:c.54_56del (IL6) XP_011513692.1:p.Leu19del
NM_000600.5:c.54_56del (IL6) MANE Select NP_000591.1:p.Leu19del
NM_001318095.2:c.-19+197_-19+199del (IL6) NP_001305024.1:n.-19+197_-19+199del
NM_001371096.1:c.20-35_20-33del (IL6) NP_001358025.1:n.20-35_20-33del