Canonical Allele Identifier: CA129768

Gene: ARID1B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206470A>T , CM000668.2:g.157206470A>T	GRCh38
NC_000006.11:g.157527604A>T , CM000668.1:g.157527604A>T	GRCh37
NC_000006.10:g.157569296A>T	NCBI36
NG_032093.1:g.433541A>T
NG_032093.2:g.433541A>T
NG_066624.1:g.435445A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5539A>T	ENSP00000055163.8:p.Lys1847Ter
ENST00000414678.8:c.5608A>T	ENSP00000412835.3:p.Lys1870Ter
ENST00000637015.2:c.5827A>T	ENSP00000489729.2:p.Lys1943Ter
ENST00000346085.10:c.5578A>T	ENSP00000344546.5:p.Lys1860Ter
ENST00000350026.10:c.5290A>T	ENSP00000055163.7:p.Lys1764Ter
ENST00000414678.7:c.3856A>T	ENSP00000412835.2:p.Lys1286Ter
ENST00000635849.1:c.3019A>T	ENSP00000490948.1:p.Lys1007Ter
ENST00000635957.1:c.2650A>T	ENSP00000490385.1:p.Lys884Ter
ENST00000636227.1:n.4161A>T
ENST00000636254.1:n.1618A>T
ENST00000636930.2:c.5698A>T MANE Select	ENSP00000490491.2:p.Lys1900Ter
ENST00000636940.1:n.3695A>T
ENST00000637015.1:c.3066A>T
ENST00000637568.1:c.2980A>T
ENST00000637741.1:n.2364A>T
ENST00000637810.1:c.3040A>T	ENSP00000489636.1:p.Lys1014Ter
ENST00000637904.1:c.3199A>T	ENSP00000490550.1:p.Lys1067Ter
ENST00000637933.1:n.2813A>T
ENST00000647938.1:c.5329A>T	ENSP00000498155.1:p.Lys1777Ter
ENST00000346085.9:c.5329A>T	ENSP00000344546.4:p.Lys1777Ter
ENST00000350026.9:c.5290A>T	ENSP00000055163.7:p.Lys1764Ter
ENST00000414678.6:c.3856A>T	ENSP00000412835.2:p.Lys1286Ter
NM_017519.2:c.5290A>T	NP_059989.2:p.Lys1764Ter
NM_020732.3:c.5329A>T	NP_065783.3:p.Lys1777Ter
XM_005267069.3:c.5449A>T	XP_005267126.2:p.Lys1817Ter
XM_011535984.1:c.4528A>T	XP_011534286.1:p.Lys1510Ter
XM_011535985.1:c.4348A>T	XP_011534287.1:p.Lys1450Ter
XM_011535986.1:c.4108A>T	XP_011534288.1:p.Lys1370Ter
XM_011535987.1:c.3727A>T	XP_011534289.1:p.Lys1243Ter
XM_011535988.1:c.2590A>T	XP_011534290.1:p.Lys864Ter
NM_001346813.1:c.5449A>T	NP_001333742.1:p.Lys1817Ter
NM_001363725.1:c.3199A>T	NP_001350654.1:p.Lys1067Ter
XM_011535984.2:c.5659A>T	XP_011534286.2:p.Lys1887Ter
XM_011535988.3:c.2590A>T	XP_011534290.1:p.Lys864Ter
XM_017011103.2:c.5560A>T	XP_016866592.1:p.Lys1854Ter
XM_017011104.1:c.5530A>T	XP_016866593.1:p.Lys1844Ter
XM_017011105.2:c.5500A>T	XP_016866594.1:p.Lys1834Ter
XM_017011106.2:c.5371A>T	XP_016866595.1:p.Lys1791Ter
XM_017011107.2:c.5350A>T	XP_016866596.1:p.Lys1784Ter
XR_002956289.1:n.5645A>T
NM_001363725.2:c.3199A>T	NP_001350654.1:p.Lys1067Ter
NM_001371656.1:c.5578A>T	NP_001358585.1:p.Lys1860Ter
NM_001374820.1:c.5578A>T	NP_001361749.1:p.Lys1860Ter
NM_001374828.1:c.5698A>T MANE Select	NP_001361757.1:p.Lys1900Ter
NM_017519.3:c.5539A>T	NP_059989.3:p.Lys1847Ter