Canonical Allele Identifier: CA4067690

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200939G>A , CM000668.2:g.157200939G>A	GRCh38
NC_000006.11:g.157522073G>A , CM000668.1:g.157522073G>A	GRCh37
NC_000006.10:g.157563765G>A	NCBI36
NG_032093.1:g.428010G>A
NG_032093.2:g.428010G>A
NG_066624.1:g.429914G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4714G>A MANE Select	NP_001361757.1:p.Gly1572Ser
ENST00000636930.2:c.4714G>A MANE Select	ENSP00000490491.2:p.Gly1572Ser
NM_001346813.1:c.4465G>A	NP_001333742.1:p.Gly1489Ser
NM_001363725.1:c.2215G>A	NP_001350654.1:p.Gly739Ser
NM_001363725.2:c.2215G>A	NP_001350654.1:p.Gly739Ser
NM_001371656.1:c.4594G>A	NP_001358585.1:p.Gly1532Ser
NM_001374820.1:c.4594G>A	NP_001361749.1:p.Gly1532Ser
NM_017519.2:c.4306G>A	NP_059989.2:p.Gly1436Ser
NM_017519.3:c.4555G>A	NP_059989.3:p.Gly1519Ser
NM_020732.3:c.4345G>A	NP_065783.3:p.Gly1449Ser
ENST00000346085.10:c.4594G>A	ENSP00000344546.5:p.Gly1532Ser
ENST00000346085.9:c.4345G>A	ENSP00000344546.4:p.Gly1449Ser
ENST00000350026.10:c.4306G>A	ENSP00000055163.7:p.Gly1436Ser
ENST00000350026.11:c.4555G>A	ENSP00000055163.8:p.Gly1519Ser
ENST00000350026.9:c.4306G>A	ENSP00000055163.7:p.Gly1436Ser
ENST00000414678.6:c.2872G>A	ENSP00000412835.2:p.Gly958Ser
ENST00000414678.7:c.2872G>A	ENSP00000412835.2:p.Gly958Ser
ENST00000414678.8:c.4624G>A	ENSP00000412835.3:p.Gly1542Ser
ENST00000635849.1:c.2035G>A	ENSP00000490948.1:p.Gly679Ser
ENST00000635957.1:c.1666G>A	ENSP00000490385.1:p.Gly556Ser
ENST00000636227.1:n.3177G>A
ENST00000636254.1:n.634G>A
ENST00000636940.1:n.2711G>A
ENST00000637015.1:c.2082G>A
ENST00000637015.2:c.4843G>A	ENSP00000489729.2:p.Gly1615Ser
ENST00000637568.1:c.1996G>A
ENST00000637741.1:n.1380G>A
ENST00000637810.1:c.2056G>A	ENSP00000489636.1:p.Gly686Ser
ENST00000637904.1:c.2215G>A	ENSP00000490550.1:p.Gly739Ser
ENST00000647938.1:c.4345G>A	ENSP00000498155.1:p.Gly1449Ser
XM_005267069.3:c.4465G>A	XP_005267126.2:p.Gly1489Ser
XM_011535984.1:c.3544G>A	XP_011534286.1:p.Gly1182Ser
XM_011535984.2:c.4675G>A	XP_011534286.2:p.Gly1559Ser
XM_011535985.1:c.3364G>A	XP_011534287.1:p.Gly1122Ser
XM_011535986.1:c.3124G>A	XP_011534288.1:p.Gly1042Ser
XM_011535987.1:c.2743G>A	XP_011534289.1:p.Gly915Ser
XM_011535988.1:c.1606G>A	XP_011534290.1:p.Gly536Ser
XM_011535988.3:c.1606G>A	XP_011534290.1:p.Gly536Ser
XM_017011103.2:c.4576G>A	XP_016866592.1:p.Gly1526Ser
XM_017011104.1:c.4546G>A	XP_016866593.1:p.Gly1516Ser
XM_017011105.2:c.4516G>A	XP_016866594.1:p.Gly1506Ser
XM_017011106.2:c.4387G>A	XP_016866595.1:p.Gly1463Ser
XM_017011107.2:c.4366G>A	XP_016866596.1:p.Gly1456Ser
XR_002956289.1:n.4661G>A