Canonical Allele Identifier: CA366248221

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207183G>A , CM000668.2:g.157207183G>A	GRCh38
NC_000006.11:g.157528317G>A , CM000668.1:g.157528317G>A	GRCh37
NC_000006.10:g.157570009G>A	NCBI36
NG_032093.1:g.434254G>A
NG_032093.2:g.434254G>A
NG_066624.1:g.436158G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.6411G>A MANE Select	NP_001361757.1:p.Trp2137Ter
ENST00000636930.2:c.6411G>A MANE Select	ENSP00000490491.2:p.Trp2137Ter
NM_001346813.1:c.6162G>A	NP_001333742.1:p.Trp2054Ter
NM_001363725.1:c.3912G>A	NP_001350654.1:p.Trp1304Ter
NM_001363725.2:c.3912G>A	NP_001350654.1:p.Trp1304Ter
NM_001371656.1:c.6291G>A	NP_001358585.1:p.Trp2097Ter
NM_001374820.1:c.6291G>A	NP_001361749.1:p.Trp2097Ter
NM_017519.2:c.6003G>A	NP_059989.2:p.Trp2001Ter
NM_017519.3:c.6252G>A	NP_059989.3:p.Trp2084Ter
NM_020732.3:c.6042G>A	NP_065783.3:p.Trp2014Ter
ENST00000346085.10:c.6291G>A	ENSP00000344546.5:p.Trp2097Ter
ENST00000346085.9:c.6042G>A	ENSP00000344546.4:p.Trp2014Ter
ENST00000350026.10:c.6003G>A	ENSP00000055163.7:p.Trp2001Ter
ENST00000350026.11:c.6252G>A	ENSP00000055163.8:p.Trp2084Ter
ENST00000350026.9:c.6003G>A	ENSP00000055163.7:p.Trp2001Ter
ENST00000414678.6:c.4569G>A	ENSP00000412835.2:p.Trp1523Ter
ENST00000414678.7:c.4569G>A	ENSP00000412835.2:p.Trp1523Ter
ENST00000414678.8:c.6321G>A	ENSP00000412835.3:p.Trp2107Ter
ENST00000635849.1:c.3732G>A	ENSP00000490948.1:p.Trp1244Ter
ENST00000635928.1:c.567G>A	ENSP00000489717.1:p.Trp189Ter
ENST00000635957.1:c.3363G>A	ENSP00000490385.1:p.Trp1121Ter
ENST00000636227.1:n.4874G>A
ENST00000636254.1:n.2331G>A
ENST00000636940.1:n.4408G>A
ENST00000637015.1:c.3779G>A
ENST00000637015.2:c.6540G>A	ENSP00000489729.2:p.Trp2180Ter
ENST00000637568.1:c.3693G>A
ENST00000637741.1:n.3077G>A
ENST00000637810.1:c.3753G>A	ENSP00000489636.1:p.Trp1251Ter
ENST00000637904.1:c.3912G>A	ENSP00000490550.1:p.Trp1304Ter
ENST00000637933.1:n.3526G>A
ENST00000647938.1:c.6042G>A	ENSP00000498155.1:p.Trp2014Ter
XM_005267069.3:c.6162G>A	XP_005267126.2:p.Trp2054Ter
XM_011535984.1:c.5241G>A	XP_011534286.1:p.Trp1747Ter
XM_011535984.2:c.6372G>A	XP_011534286.2:p.Trp2124Ter
XM_011535985.1:c.5061G>A	XP_011534287.1:p.Trp1687Ter
XM_011535986.1:c.4821G>A	XP_011534288.1:p.Trp1607Ter
XM_011535987.1:c.4440G>A	XP_011534289.1:p.Trp1480Ter
XM_011535988.1:c.3303G>A	XP_011534290.1:p.Trp1101Ter
XM_011535988.3:c.3303G>A	XP_011534290.1:p.Trp1101Ter
XM_017011103.2:c.6273G>A	XP_016866592.1:p.Trp2091Ter
XM_017011104.1:c.6243G>A	XP_016866593.1:p.Trp2081Ter
XM_017011105.2:c.6213G>A	XP_016866594.1:p.Trp2071Ter
XM_017011106.2:c.6084G>A	XP_016866595.1:p.Trp2028Ter
XM_017011107.2:c.6063G>A	XP_016866596.1:p.Trp2021Ter
XR_002956289.1:n.6358G>A