Canonical Allele Identifier: CA359779122

Gene: IL6ST

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55941609T>G , CM000667.2:g.55941609T>G	GRCh38
NC_000005.9:g.55237437T>G , CM000667.1:g.55237437T>G	GRCh37
NC_000005.8:g.55273194T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381294.8:c.2047A>C	ENSP00000370694.3:p.Ser683Arg
ENST00000506241.2:n.3571A>C
ENST00000577363.2:c.*1635A>C	ENSP00000513861.1:n.*1635A>C
ENST00000698638.1:c.1327A>C	ENSP00000513851.1:p.Ser443Arg
ENST00000698639.1:c.2083A>C	ENSP00000513852.1:p.Ser695Arg
ENST00000698640.1:c.1513A>C	ENSP00000513853.1:n.1513A>C
ENST00000698641.1:c.*1452A>C	ENSP00000513854.1:n.*1452A>C
ENST00000698642.1:c.*1681A>C	ENSP00000513855.1:n.*1681A>C
ENST00000698643.1:c.*1552A>C	ENSP00000513856.1:n.*1552A>C
ENST00000698644.1:c.2020A>C	ENSP00000513857.1:p.Ser674Arg
ENST00000698645.1:c.2230A>C	ENSP00000513858.1:p.Ser744Arg
ENST00000698646.1:c.2128A>C	ENSP00000513859.1:p.Ser710Arg
ENST00000698647.1:c.*1849A>C	ENSP00000513860.1:n.*1849A>C
ENST00000698648.1:c.*1635A>C	ENSP00000513862.1:n.*1635A>C
ENST00000698649.1:n.1232A>C
ENST00000381298.7:c.2230A>C MANE Select	ENSP00000370698.2:p.Ser744Arg
ENST00000651614.1:c.*1182A>C	ENSP00000498224.1:n.*1182A>C
ENST00000336909.9:c.2230A>C	ENSP00000338799.5:p.Ser744Arg
ENST00000381287.8:c.*1157A>C	ENSP00000370687.4:n.*1157A>C
ENST00000381294.7:c.2047A>C	ENSP00000370694.3:p.Ser683Arg
ENST00000381298.6:c.2230A>C	ENSP00000370698.2:p.Ser744Arg
ENST00000502326.7:c.2230A>C	ENSP00000462158.1:p.Ser744Arg
ENST00000503773.6:c.*1274A>C	ENSP00000426224.2:n.*1274A>C
ENST00000523039.5:n.395A>C
NM_001190981.1:c.2047A>C	NP_001177910.1:p.Ser683Arg
NM_002184.3:c.2230A>C	NP_002175.2:p.Ser744Arg
NM_175767.2:c.*1157A>C	NP_786943.1:n.*1157A>C
NR_120480.1:n.2589A>C
NM_001364275.1:c.2128A>C	NP_001351204.1:p.Ser710Arg
NM_001364276.1:c.2020A>C	NP_001351205.1:p.Ser674Arg
NM_001364277.1:c.1363A>C	NP_001351206.1:p.Ser455Arg
NM_001364278.1:c.1327A>C	NP_001351207.1:p.Ser443Arg
NM_001364279.1:c.1234A>C	NP_001351208.1:p.Ser412Arg
NR_157112.1:n.3394A>C
NM_002184.4:c.2230A>C MANE Select	NP_002175.2:p.Ser744Arg
NM_001190981.2:c.2047A>C	NP_001177910.1:p.Ser683Arg
NM_001364275.2:c.2128A>C	NP_001351204.1:p.Ser710Arg
NM_001364276.2:c.2020A>C	NP_001351205.1:p.Ser674Arg
NM_001364277.2:c.1363A>C	NP_001351206.1:p.Ser455Arg
NM_001364278.2:c.1327A>C	NP_001351207.1:p.Ser443Arg
NM_001364279.2:c.1234A>C	NP_001351208.1:p.Ser412Arg
NM_175767.3:c.*1157A>C	NP_786943.1:n.*1157A>C
NR_120480.2:n.2559A>C
NR_157112.2:n.3394A>C