Canonical Allele Identifier: CA1547714971
Gene: IL6ST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55954899A= , CM000667.2:g.55954899A= GRCh38
NC_000005.9:g.55250727A= , CM000667.1:g.55250727A= GRCh37
NC_000005.8:g.55286484A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002184.4:c.1361T= MANE Select NP_002175.2:p.Ile454=
ENST00000381298.7:c.1361T= MANE Select ENSP00000370698.2:p.Ile454=
NM_001190981.1:c.1267+1126T= NP_001177910.1:n.1267+1126T=
NM_001190981.2:c.1267+1126T= NP_001177910.1:n.1267+1126T=
NM_001364275.1:c.1361T= NP_001351204.1:p.Ile454=
NM_001364275.2:c.1361T= NP_001351204.1:p.Ile454=
NM_001364276.1:c.1151T= NP_001351205.1:p.Ile384=
NM_001364276.2:c.1151T= NP_001351205.1:p.Ile384=
NM_001364277.1:c.494T= NP_001351206.1:p.Ile165=
NM_001364277.2:c.494T= NP_001351206.1:p.Ile165=
NM_001364278.1:c.458T= NP_001351207.1:p.Ile153=
NM_001364278.2:c.458T= NP_001351207.1:p.Ile153=
NM_001364279.1:c.365T= NP_001351208.1:p.Ile122=
NM_001364279.2:c.365T= NP_001351208.1:p.Ile122=
NM_002184.3:c.1361T= NP_002175.2:p.Ile454=
NM_175767.2:c.*288T= NP_786943.1:n.*288T=
NM_175767.3:c.*288T= NP_786943.1:n.*288T=
NR_120480.1:n.1720T=
NR_120480.2:n.1690T=
NR_157112.1:n.1644T=
NR_157112.2:n.1644T=
ENST00000336909.9:c.1361T= ENSP00000338799.5:p.Ile454=
ENST00000381286.7:c.65-12148T= ENSP00000370686.3:n.65-12148T=
ENST00000381287.8:c.*288T= ENSP00000370687.4:n.*288T=
ENST00000381293.6:c.475+5503T= ENSP00000370693.2:n.475+5503T=
ENST00000381294.7:c.1267+1126T= ENSP00000370694.3:n.1267+1126T=
ENST00000381294.8:c.1267+1126T= ENSP00000370694.3:n.1267+1126T=
ENST00000381298.6:c.1361T= ENSP00000370698.2:p.Ile454=
ENST00000502326.7:c.1361T= ENSP00000462158.1:p.Ile454=
ENST00000503773.6:c.*405T= ENSP00000426224.2:n.*405T=
ENST00000506241.2:n.2702T=
ENST00000522633.2:c.*288T= ENSP00000435399.1:n.*288T=
ENST00000577363.2:c.*766T= ENSP00000513861.1:n.*766T=
ENST00000651614.1:c.1361T= ENSP00000498224.1:p.Ile454=
ENST00000698638.1:c.458T= ENSP00000513851.1:p.Ile153=
ENST00000698639.1:c.1361T= ENSP00000513852.1:p.Ile454=
ENST00000698640.1:c.733+1126T= ENSP00000513853.1:n.733+1126T=
ENST00000698641.1:c.*672+1126T= ENSP00000513854.1:n.*672+1126T=
ENST00000698642.1:c.*812T= ENSP00000513855.1:n.*812T=
ENST00000698643.1:c.*683T= ENSP00000513856.1:n.*683T=
ENST00000698644.1:c.1151T= ENSP00000513857.1:p.Ile384=
ENST00000698645.1:c.1361T= ENSP00000513858.1:p.Ile454=
ENST00000698646.1:c.1361T= ENSP00000513859.1:p.Ile454=
ENST00000698647.1:c.*980T= ENSP00000513860.1:n.*980T=
ENST00000698648.1:c.*766T= ENSP00000513862.1:n.*766T=
XM_011543376.1:c.1361T= XP_011541678.1:p.Ile454=