Canonical Allele Identifier: CA11968995

Gene: IL6ST

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55966832A>G , CM000667.2:g.55966832A>G	GRCh38
NC_000005.9:g.55262660A>G , CM000667.1:g.55262660A>G	GRCh37
NC_000005.8:g.55298417A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381294.8:c.491+1444T>C	ENSP00000370694.3:n.491+1444T>C
ENST00000506241.2:n.800+1444T>C
ENST00000577363.2:c.65-2520T>C	ENSP00000513861.1:n.65-2520T>C
ENST00000698638.1:c.-90-6271T>C	ENSP00000513851.1:n.-90-6271T>C
ENST00000698639.1:c.491+1444T>C	ENSP00000513852.1:n.491+1444T>C
ENST00000698640.1:c.41-2520T>C	ENSP00000513853.1:n.41-2520T>C
ENST00000698641.1:c.65-2520T>C	ENSP00000513854.1:n.65-2520T>C
ENST00000698642.1:c.371-2520T>C	ENSP00000513855.1:n.371-2520T>C
ENST00000698643.1:c.371-2520T>C	ENSP00000513856.1:n.371-2520T>C
ENST00000698644.1:c.281+1444T>C	ENSP00000513857.1:n.281+1444T>C
ENST00000698645.1:c.491+1444T>C	ENSP00000513858.1:n.491+1444T>C
ENST00000698646.1:c.491+1444T>C	ENSP00000513859.1:n.491+1444T>C
ENST00000698647.1:c.*110+1444T>C	ENSP00000513860.1:n.*110+1444T>C
ENST00000698648.1:c.371-2520T>C	ENSP00000513862.1:n.371-2520T>C
ENST00000381298.7:c.491+1444T>C MANE Select	ENSP00000370698.2:n.491+1444T>C
ENST00000651614.1:c.491+1444T>C	ENSP00000498224.1:n.491+1444T>C
ENST00000336909.9:c.491+1444T>C	ENSP00000338799.5:n.491+1444T>C
ENST00000381286.7:c.64+9383T>C	ENSP00000370686.3:n.64+9383T>C
ENST00000381287.8:c.491+1444T>C	ENSP00000370687.4:n.491+1444T>C
ENST00000381293.6:c.160+2928T>C	ENSP00000370693.2:n.160+2928T>C
ENST00000381294.7:c.491+1444T>C	ENSP00000370694.3:n.491+1444T>C
ENST00000381298.6:c.491+1444T>C	ENSP00000370698.2:n.491+1444T>C
ENST00000396816.1:c.65-2520T>C	ENSP00000463896.1:n.65-2520T>C
ENST00000502326.7:c.491+1444T>C	ENSP00000462158.1:n.491+1444T>C
ENST00000503773.6:c.491+1444T>C	ENSP00000426224.2:n.491+1444T>C
ENST00000522633.2:c.491+1444T>C	ENSP00000435399.1:n.491+1444T>C
ENST00000577363.1:n.179-2520T>C
NM_001190981.1:c.491+1444T>C	NP_001177910.1:n.491+1444T>C
NM_002184.3:c.491+1444T>C	NP_002175.2:n.491+1444T>C
NM_175767.2:c.491+1444T>C	NP_786943.1:n.491+1444T>C
NR_120480.1:n.804+1444T>C
XM_011543376.1:c.491+1444T>C	XP_011541678.1:n.491+1444T>C
XM_011543377.1:c.491+1444T>C	XP_011541679.1:n.491+1444T>C
NM_001364275.1:c.491+1444T>C	NP_001351204.1:n.491+1444T>C
NM_001364276.1:c.281+1444T>C	NP_001351205.1:n.281+1444T>C
NM_001364277.1:c.-422-2520T>C	NP_001351206.1:n.-422-2520T>C
NM_001364278.1:c.-412-2520T>C	NP_001351207.1:n.-412-2520T>C
NM_001364279.1:c.-422-2520T>C	NP_001351208.1:n.-422-2520T>C
NR_157112.1:n.774+1444T>C
NM_002184.4:c.491+1444T>C MANE Select	NP_002175.2:n.491+1444T>C
NM_001190981.2:c.491+1444T>C	NP_001177910.1:n.491+1444T>C
NM_001364275.2:c.491+1444T>C	NP_001351204.1:n.491+1444T>C
NM_001364276.2:c.281+1444T>C	NP_001351205.1:n.281+1444T>C
NM_001364277.2:c.-422-2520T>C	NP_001351206.1:n.-422-2520T>C
NM_001364278.2:c.-412-2520T>C	NP_001351207.1:n.-412-2520T>C
NM_001364279.2:c.-422-2520T>C	NP_001351208.1:n.-422-2520T>C
NM_175767.3:c.491+1444T>C	NP_786943.1:n.491+1444T>C
NR_120480.2:n.774+1444T>C
NR_157112.2:n.774+1444T>C