Canonical Allele Identifier: CA1547715520
Gene: IL6ST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55956103G= , CM000667.2:g.55956103G= GRCh38
NC_000005.9:g.55251931G= , CM000667.1:g.55251931G= GRCh37
NC_000005.8:g.55287688G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381294.8:c.1189C= ENSP00000370694.3:p.Leu397=
ENST00000506241.2:n.1498C=
ENST00000577363.2:c.*594C= ENSP00000513861.1:n.*594C=
ENST00000698638.1:c.286C= ENSP00000513851.1:p.Leu96=
ENST00000698639.1:c.1189C= ENSP00000513852.1:p.Leu397=
ENST00000698640.1:c.655C= ENSP00000513853.1:n.655C=
ENST00000698641.1:c.*594C= ENSP00000513854.1:n.*594C=
ENST00000698642.1:c.*640C= ENSP00000513855.1:n.*640C=
ENST00000698643.1:c.*511C= ENSP00000513856.1:n.*511C=
ENST00000698644.1:c.979C= ENSP00000513857.1:p.Leu327=
ENST00000698645.1:c.1189C= ENSP00000513858.1:p.Leu397=
ENST00000698646.1:c.1189C= ENSP00000513859.1:p.Leu397=
ENST00000698647.1:c.*808C= ENSP00000513860.1:n.*808C=
ENST00000698648.1:c.*594C= ENSP00000513862.1:n.*594C=
ENST00000381298.7:c.1189C= MANE Select ENSP00000370698.2:p.Leu397=
ENST00000651614.1:c.1189C= ENSP00000498224.1:p.Leu397=
ENST00000336909.9:c.1189C= ENSP00000338799.5:p.Leu397=
ENST00000381286.7:c.65-13352C= ENSP00000370686.3:n.65-13352C=
ENST00000381287.8:c.*116C= ENSP00000370687.4:n.*116C=
ENST00000381293.6:c.475+4299C= ENSP00000370693.2:n.475+4299C=
ENST00000381294.7:c.1189C= ENSP00000370694.3:p.Leu397=
ENST00000381298.6:c.1189C= ENSP00000370698.2:p.Leu397=
ENST00000502326.7:c.1189C= ENSP00000462158.1:p.Leu397=
ENST00000503773.6:c.*233C= ENSP00000426224.2:n.*233C=
ENST00000506241.1:n.295C=
ENST00000522633.2:c.*116C= ENSP00000435399.1:n.*116C=
NM_001190981.1:c.1189C= NP_001177910.1:p.Leu397=
NM_002184.3:c.1189C= NP_002175.2:p.Leu397=
NM_175767.2:c.*116C= NP_786943.1:n.*116C=
NR_120480.1:n.1548C=
XM_011543376.1:c.1189C= XP_011541678.1:p.Leu397=
NM_001364275.1:c.1189C= NP_001351204.1:p.Leu397=
NM_001364276.1:c.979C= NP_001351205.1:p.Leu327=
NM_001364277.1:c.322C= NP_001351206.1:p.Leu108=
NM_001364278.1:c.286C= NP_001351207.1:p.Leu96=
NM_001364279.1:c.193C= NP_001351208.1:p.Leu65=
NR_157112.1:n.1472C=
NM_002184.4:c.1189C= MANE Select NP_002175.2:p.Leu397=
NM_001190981.2:c.1189C= NP_001177910.1:p.Leu397=
NM_001364275.2:c.1189C= NP_001351204.1:p.Leu397=
NM_001364276.2:c.979C= NP_001351205.1:p.Leu327=
NM_001364277.2:c.322C= NP_001351206.1:p.Leu108=
NM_001364278.2:c.286C= NP_001351207.1:p.Leu96=
NM_001364279.2:c.193C= NP_001351208.1:p.Leu65=
NM_175767.3:c.*116C= NP_786943.1:n.*116C=
NR_120480.2:n.1518C=
NR_157112.2:n.1472C=