Canonical Allele Identifier: CA452780812

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317589
• MyVariant Identifiers: chr6:g.157502264C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181130C>T , CM000668.2:g.157181130C>T	GRCh38
NC_000006.11:g.157502264C>T , CM000668.1:g.157502264C>T	GRCh37
NC_000006.10:g.157543956C>T	NCBI36
NG_032093.1:g.408201C>T
NG_032093.2:g.408201C>T
NG_066624.1:g.410105C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3507C>T	ENSP00000055163.8:p.Asp1169=
ENST00000414678.8:c.3576C>T	ENSP00000412835.3:p.Asp1192=
ENST00000637015.2:c.3795C>T	ENSP00000489729.2:p.Asp1265=
ENST00000319584.11:c.1680C>T	ENSP00000313006.7:p.Asp560=
ENST00000346085.10:c.3546C>T	ENSP00000344546.5:p.Asp1182=
ENST00000350026.10:c.3258C>T	ENSP00000055163.7:p.Asp1086=
ENST00000414678.7:c.1824C>T	ENSP00000412835.2:p.Asp608=
ENST00000635849.1:c.987C>T	ENSP00000490948.1:p.Asp329=
ENST00000635957.1:c.621C>T	ENSP00000490385.1:p.Asp207=
ENST00000636930.2:c.3666C>T MANE Select	ENSP00000490491.2:p.Asp1222=
ENST00000636940.1:n.1663C>T
ENST00000637015.1:c.1034C>T
ENST00000637568.1:c.948C>T
ENST00000637741.1:n.332C>T
ENST00000637810.1:c.1008C>T	ENSP00000489636.1:p.Asp336=
ENST00000637904.1:c.1167C>T	ENSP00000490550.1:p.Asp389=
ENST00000647938.1:c.3297C>T	ENSP00000498155.1:p.Asp1099=
ENST00000319584.10:c.1683C>T	ENSP00000313006.6:p.Asp561=
ENST00000346085.9:c.3297C>T	ENSP00000344546.4:p.Asp1099=
ENST00000350026.9:c.3258C>T	ENSP00000055163.7:p.Asp1086=
ENST00000400790.3:c.459C>T	ENSP00000383596.3:p.Asp153=
ENST00000414678.6:c.1824C>T	ENSP00000412835.2:p.Asp608=
ENST00000478761.3:c.868C>T
NM_017519.2:c.3258C>T	NP_059989.2:p.Asp1086=
NM_020732.3:c.3297C>T	NP_065783.3:p.Asp1099=
XM_005267069.3:c.3417C>T	XP_005267126.2:p.Asp1139=
XM_011535984.1:c.2496C>T	XP_011534286.1:p.Asp832=
XM_011535985.1:c.2316C>T	XP_011534287.1:p.Asp772=
XM_011535986.1:c.2076C>T	XP_011534288.1:p.Asp692=
XM_011535987.1:c.1695C>T	XP_011534289.1:p.Asp565=
XM_011535988.1:c.558C>T	XP_011534290.1:p.Asp186=
NM_001346813.1:c.3417C>T	NP_001333742.1:p.Asp1139=
NM_001363725.1:c.1167C>T	NP_001350654.1:p.Asp389=
XM_011535984.2:c.3627C>T	XP_011534286.2:p.Asp1209=
XM_011535988.3:c.558C>T	XP_011534290.1:p.Asp186=
XM_017011103.2:c.3528C>T	XP_016866592.1:p.Asp1176=
XM_017011104.1:c.3498C>T	XP_016866593.1:p.Asp1166=
XM_017011105.2:c.3468C>T	XP_016866594.1:p.Asp1156=
XM_017011106.2:c.3339C>T	XP_016866595.1:p.Asp1113=
XM_017011107.2:c.3318C>T	XP_016866596.1:p.Asp1106=
XR_002956289.1:n.3710C>T
NM_001363725.2:c.1167C>T	NP_001350654.1:p.Asp389=
NM_001371656.1:c.3546C>T	NP_001358585.1:p.Asp1182=
NM_001374820.1:c.3546C>T	NP_001361749.1:p.Asp1182=
NM_001374828.1:c.3666C>T MANE Select	NP_001361757.1:p.Asp1222=
NM_017519.3:c.3507C>T	NP_059989.3:p.Asp1169=