Canonical Allele Identifier: CA366246934

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206597G>A , CM000668.2:g.157206597G>A	GRCh38
NC_000006.11:g.157527731G>A , CM000668.1:g.157527731G>A	GRCh37
NC_000006.10:g.157569423G>A	NCBI36
NG_032093.1:g.433668G>A
NG_032093.2:g.433668G>A
NG_066624.1:g.435572G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.5825G>A MANE Select	NP_001361757.1:p.Trp1942Ter
ENST00000636930.2:c.5825G>A MANE Select	ENSP00000490491.2:p.Trp1942Ter
NM_001346813.1:c.5576G>A	NP_001333742.1:p.Trp1859Ter
NM_001363725.1:c.3326G>A	NP_001350654.1:p.Trp1109Ter
NM_001363725.2:c.3326G>A	NP_001350654.1:p.Trp1109Ter
NM_001371656.1:c.5705G>A	NP_001358585.1:p.Trp1902Ter
NM_001374820.1:c.5705G>A	NP_001361749.1:p.Trp1902Ter
NM_017519.2:c.5417G>A	NP_059989.2:p.Trp1806Ter
NM_017519.3:c.5666G>A	NP_059989.3:p.Trp1889Ter
NM_020732.3:c.5456G>A	NP_065783.3:p.Trp1819Ter
ENST00000346085.10:c.5705G>A	ENSP00000344546.5:p.Trp1902Ter
ENST00000346085.9:c.5456G>A	ENSP00000344546.4:p.Trp1819Ter
ENST00000350026.10:c.5417G>A	ENSP00000055163.7:p.Trp1806Ter
ENST00000350026.11:c.5666G>A	ENSP00000055163.8:p.Trp1889Ter
ENST00000350026.9:c.5417G>A	ENSP00000055163.7:p.Trp1806Ter
ENST00000414678.6:c.3983G>A	ENSP00000412835.2:p.Trp1328Ter
ENST00000414678.7:c.3983G>A	ENSP00000412835.2:p.Trp1328Ter
ENST00000414678.8:c.5735G>A	ENSP00000412835.3:p.Trp1912Ter
ENST00000635849.1:c.3146G>A	ENSP00000490948.1:p.Trp1049Ter
ENST00000635957.1:c.2777G>A	ENSP00000490385.1:p.Trp926Ter
ENST00000636227.1:n.4288G>A
ENST00000636254.1:n.1745G>A
ENST00000636940.1:n.3822G>A
ENST00000637015.1:c.3193G>A
ENST00000637015.2:c.5954G>A	ENSP00000489729.2:p.Trp1985Ter
ENST00000637568.1:c.3107G>A
ENST00000637741.1:n.2491G>A
ENST00000637810.1:c.3167G>A	ENSP00000489636.1:p.Trp1056Ter
ENST00000637904.1:c.3326G>A	ENSP00000490550.1:p.Trp1109Ter
ENST00000637933.1:n.2940G>A
ENST00000647938.1:c.5456G>A	ENSP00000498155.1:p.Trp1819Ter
XM_005267069.3:c.5576G>A	XP_005267126.2:p.Trp1859Ter
XM_011535984.1:c.4655G>A	XP_011534286.1:p.Trp1552Ter
XM_011535984.2:c.5786G>A	XP_011534286.2:p.Trp1929Ter
XM_011535985.1:c.4475G>A	XP_011534287.1:p.Trp1492Ter
XM_011535986.1:c.4235G>A	XP_011534288.1:p.Trp1412Ter
XM_011535987.1:c.3854G>A	XP_011534289.1:p.Trp1285Ter
XM_011535988.1:c.2717G>A	XP_011534290.1:p.Trp906Ter
XM_011535988.3:c.2717G>A	XP_011534290.1:p.Trp906Ter
XM_017011103.2:c.5687G>A	XP_016866592.1:p.Trp1896Ter
XM_017011104.1:c.5657G>A	XP_016866593.1:p.Trp1886Ter
XM_017011105.2:c.5627G>A	XP_016866594.1:p.Trp1876Ter
XM_017011106.2:c.5498G>A	XP_016866595.1:p.Trp1833Ter
XM_017011107.2:c.5477G>A	XP_016866596.1:p.Trp1826Ter
XR_002956289.1:n.5772G>A