Canonical Allele Identifier: CA359777895

Gene: IL6ST

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55941313C>G , CM000667.2:g.55941313C>G	GRCh38
NC_000005.9:g.55237141C>G , CM000667.1:g.55237141C>G	GRCh37
NC_000005.8:g.55272898C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002184.4:c.2526G>C MANE Select	NP_002175.2:p.Glu842Asp
ENST00000381298.7:c.2526G>C MANE Select	ENSP00000370698.2:p.Glu842Asp
NM_001190981.1:c.2343G>C	NP_001177910.1:p.Glu781Asp
NM_001190981.2:c.2343G>C	NP_001177910.1:p.Glu781Asp
NM_001364275.1:c.2424G>C	NP_001351204.1:p.Glu808Asp
NM_001364275.2:c.2424G>C	NP_001351204.1:p.Glu808Asp
NM_001364276.1:c.2316G>C	NP_001351205.1:p.Glu772Asp
NM_001364276.2:c.2316G>C	NP_001351205.1:p.Glu772Asp
NM_001364277.1:c.1659G>C	NP_001351206.1:p.Glu553Asp
NM_001364277.2:c.1659G>C	NP_001351206.1:p.Glu553Asp
NM_001364278.1:c.1623G>C	NP_001351207.1:p.Glu541Asp
NM_001364278.2:c.1623G>C	NP_001351207.1:p.Glu541Asp
NM_001364279.1:c.1530G>C	NP_001351208.1:p.Glu510Asp
NM_001364279.2:c.1530G>C	NP_001351208.1:p.Glu510Asp
NM_002184.3:c.2526G>C	NP_002175.2:p.Glu842Asp
NM_175767.2:c.*1453G>C	NP_786943.1:n.*1453G>C
NM_175767.3:c.*1453G>C	NP_786943.1:n.*1453G>C
NR_120480.1:n.2885G>C
NR_120480.2:n.2855G>C
NR_157112.1:n.3690G>C
NR_157112.2:n.3690G>C
ENST00000336909.9:c.2526G>C	ENSP00000338799.5:p.Glu842Asp
ENST00000381287.8:c.*1453G>C	ENSP00000370687.4:n.*1453G>C
ENST00000381294.7:c.2343G>C	ENSP00000370694.3:p.Glu781Asp
ENST00000381294.8:c.2343G>C	ENSP00000370694.3:p.Glu781Asp
ENST00000381298.6:c.2526G>C	ENSP00000370698.2:p.Glu842Asp
ENST00000502326.7:c.2526G>C	ENSP00000462158.1:p.Glu842Asp
ENST00000503773.6:c.*1570G>C	ENSP00000426224.2:n.*1570G>C
ENST00000506241.2:n.3867G>C
ENST00000577363.2:c.*1931G>C	ENSP00000513861.1:n.*1931G>C
ENST00000651614.1:c.*1478G>C	ENSP00000498224.1:n.*1478G>C
ENST00000698638.1:c.1623G>C	ENSP00000513851.1:p.Glu541Asp
ENST00000698639.1:c.2379G>C	ENSP00000513852.1:p.Glu793Asp
ENST00000698640.1:c.1809G>C	ENSP00000513853.1:n.1809G>C
ENST00000698641.1:c.*1748G>C	ENSP00000513854.1:n.*1748G>C
ENST00000698642.1:c.*1977G>C	ENSP00000513855.1:n.*1977G>C
ENST00000698643.1:c.*1848G>C	ENSP00000513856.1:n.*1848G>C
ENST00000698644.1:c.2316G>C	ENSP00000513857.1:p.Glu772Asp
ENST00000698645.1:c.2526G>C	ENSP00000513858.1:p.Glu842Asp
ENST00000698646.1:c.2424G>C	ENSP00000513859.1:p.Glu808Asp
ENST00000698647.1:c.*2145G>C	ENSP00000513860.1:n.*2145G>C
ENST00000698648.1:c.*1931G>C	ENSP00000513862.1:n.*1931G>C
ENST00000698649.1:n.1528G>C