Canonical Allele Identifier: CA3271110

Gene: IL6ST

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55941137A>G , CM000667.2:g.55941137A>G	GRCh38
NC_000005.9:g.55236965A>G , CM000667.1:g.55236965A>G	GRCh37
NC_000005.8:g.55272722A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002184.4:c.2702T>C MANE Select	NP_002175.2:p.Met901Thr
ENST00000381298.7:c.2702T>C MANE Select	ENSP00000370698.2:p.Met901Thr
NM_001190981.1:c.2519T>C	NP_001177910.1:p.Met840Thr
NM_001190981.2:c.2519T>C	NP_001177910.1:p.Met840Thr
NM_001364275.1:c.2600T>C	NP_001351204.1:p.Met867Thr
NM_001364275.2:c.2600T>C	NP_001351204.1:p.Met867Thr
NM_001364276.1:c.2492T>C	NP_001351205.1:p.Met831Thr
NM_001364276.2:c.2492T>C	NP_001351205.1:p.Met831Thr
NM_001364277.1:c.1835T>C	NP_001351206.1:p.Met612Thr
NM_001364277.2:c.1835T>C	NP_001351206.1:p.Met612Thr
NM_001364278.1:c.1799T>C	NP_001351207.1:p.Met600Thr
NM_001364278.2:c.1799T>C	NP_001351207.1:p.Met600Thr
NM_001364279.1:c.1706T>C	NP_001351208.1:p.Met569Thr
NM_001364279.2:c.1706T>C	NP_001351208.1:p.Met569Thr
NM_002184.3:c.2702T>C	NP_002175.2:p.Met901Thr
NM_175767.2:c.*1629T>C	NP_786943.1:n.*1629T>C
NM_175767.3:c.*1629T>C	NP_786943.1:n.*1629T>C
NR_120480.1:n.3061T>C
NR_120480.2:n.3031T>C
NR_157112.1:n.3866T>C
NR_157112.2:n.3866T>C
ENST00000336909.9:c.2702T>C	ENSP00000338799.5:p.Met901Thr
ENST00000381287.8:c.*1629T>C	ENSP00000370687.4:n.*1629T>C
ENST00000381294.7:c.2519T>C	ENSP00000370694.3:p.Met840Thr
ENST00000381294.8:c.2519T>C	ENSP00000370694.3:p.Met840Thr
ENST00000381298.6:c.2702T>C	ENSP00000370698.2:p.Met901Thr
ENST00000502326.7:c.2702T>C	ENSP00000462158.1:p.Met901Thr
ENST00000503773.6:c.*1746T>C	ENSP00000426224.2:n.*1746T>C
ENST00000506241.2:n.4043T>C
ENST00000577363.2:c.*2107T>C	ENSP00000513861.1:n.*2107T>C
ENST00000651614.1:c.*1654T>C	ENSP00000498224.1:n.*1654T>C
ENST00000698638.1:c.1799T>C	ENSP00000513851.1:p.Met600Thr
ENST00000698639.1:c.2555T>C	ENSP00000513852.1:p.Met852Thr
ENST00000698640.1:c.1985T>C	ENSP00000513853.1:n.1985T>C
ENST00000698641.1:c.*1924T>C	ENSP00000513854.1:n.*1924T>C
ENST00000698642.1:c.*2153T>C	ENSP00000513855.1:n.*2153T>C
ENST00000698643.1:c.*2024T>C	ENSP00000513856.1:n.*2024T>C
ENST00000698644.1:c.2492T>C	ENSP00000513857.1:p.Met831Thr
ENST00000698645.1:c.2702T>C	ENSP00000513858.1:p.Met901Thr
ENST00000698646.1:c.2600T>C	ENSP00000513859.1:p.Met867Thr
ENST00000698647.1:c.*2321T>C	ENSP00000513860.1:n.*2321T>C
ENST00000698648.1:c.*2107T>C	ENSP00000513862.1:n.*2107T>C
ENST00000698649.1:n.1704T>C