Canonical Allele Identifier: CA1694105832
Gene: IL6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22730530G>C , CM000669.2:g.22730530G>C GRCh38
NC_000007.13:g.22770149G>C , CM000669.1:g.22770149G>C GRCh37
NC_000007.12:g.22736674G>C NCBI36
NG_011640.1:g.8384G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000464710.2:n.2647G>C
ENST00000258743.10:c.471+870G>C MANE Select ENSP00000258743.5:n.471+870G>C
ENST00000258743.9:c.471+870G>C ENSP00000258743.5:n.471+870G>C
ENST00000401630.7:c.402+870G>C ENSP00000384928.3:n.402+870G>C
ENST00000404625.5:c.471+870G>C ENSP00000385675.1:n.471+870G>C
ENST00000407492.5:c.243+870G>C ENSP00000385043.1:n.243+870G>C
ENST00000485300.1:n.696+870G>C
NM_000600.3:c.471+870G>C NP_000591.1:n.471+870G>C
XM_005249745.3:c.*744G>C XP_005249802.1:n.*744G>C
XM_011515390.1:c.471+870G>C XP_011513692.1:n.471+870G>C
XM_011515391.1:c.243+870G>C XP_011513693.1:n.243+870G>C
NM_000600.4:c.471+870G>C NP_000591.1:n.471+870G>C
NM_001318095.1:c.243+870G>C NP_001305024.1:n.243+870G>C
XM_005249745.5:c.*744G>C XP_005249802.1:n.*744G>C
XM_011515390.2:c.471+870G>C XP_011513692.1:n.471+870G>C
NM_000600.5:c.471+870G>C MANE Select NP_000591.1:n.471+870G>C
NM_001318095.2:c.243+870G>C NP_001305024.1:n.243+870G>C
NM_001371096.1:c.402+870G>C NP_001358025.1:n.402+870G>C