Canonical Allele Identifier: CA452780771

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317182
• MyVariant Identifiers: chr6:g.157502201C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181067C>A , CM000668.2:g.157181067C>A	GRCh38
NC_000006.11:g.157502201C>A , CM000668.1:g.157502201C>A	GRCh37
NC_000006.10:g.157543893C>A	NCBI36
NG_032093.1:g.408138C>A
NG_032093.2:g.408138C>A
NG_066624.1:g.410042C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3444C>A	ENSP00000055163.8:p.Thr1148=
ENST00000414678.8:c.3513C>A	ENSP00000412835.3:p.Thr1171=
ENST00000637015.2:c.3732C>A	ENSP00000489729.2:p.Thr1244=
ENST00000319584.11:c.1617C>A	ENSP00000313006.7:p.Thr539=
ENST00000346085.10:c.3483C>A	ENSP00000344546.5:p.Thr1161=
ENST00000350026.10:c.3195C>A	ENSP00000055163.7:p.Thr1065=
ENST00000414678.7:c.1761C>A	ENSP00000412835.2:p.Thr587=
ENST00000635849.1:c.924C>A	ENSP00000490948.1:p.Thr308=
ENST00000635957.1:c.558C>A	ENSP00000490385.1:p.Thr186=
ENST00000636930.2:c.3603C>A MANE Select	ENSP00000490491.2:p.Thr1201=
ENST00000636940.1:n.1600C>A
ENST00000637015.1:c.971C>A
ENST00000637568.1:c.885C>A
ENST00000637741.1:n.269C>A
ENST00000637810.1:c.945C>A	ENSP00000489636.1:p.Thr315=
ENST00000637904.1:c.1104C>A	ENSP00000490550.1:p.Thr368=
ENST00000647938.1:c.3234C>A	ENSP00000498155.1:p.Thr1078=
ENST00000319584.10:c.1620C>A	ENSP00000313006.6:p.Thr540=
ENST00000346085.9:c.3234C>A	ENSP00000344546.4:p.Thr1078=
ENST00000350026.9:c.3195C>A	ENSP00000055163.7:p.Thr1065=
ENST00000400790.3:c.396C>A	ENSP00000383596.3:p.Thr132=
ENST00000414678.6:c.1761C>A	ENSP00000412835.2:p.Thr587=
ENST00000478761.3:c.805C>A
NM_017519.2:c.3195C>A	NP_059989.2:p.Thr1065=
NM_020732.3:c.3234C>A	NP_065783.3:p.Thr1078=
XM_005267069.3:c.3354C>A	XP_005267126.2:p.Thr1118=
XM_011535984.1:c.2433C>A	XP_011534286.1:p.Thr811=
XM_011535985.1:c.2253C>A	XP_011534287.1:p.Thr751=
XM_011535986.1:c.2013C>A	XP_011534288.1:p.Thr671=
XM_011535987.1:c.1632C>A	XP_011534289.1:p.Thr544=
XM_011535988.1:c.495C>A	XP_011534290.1:p.Thr165=
NM_001346813.1:c.3354C>A	NP_001333742.1:p.Thr1118=
NM_001363725.1:c.1104C>A	NP_001350654.1:p.Thr368=
XM_011535984.2:c.3564C>A	XP_011534286.2:p.Thr1188=
XM_011535988.3:c.495C>A	XP_011534290.1:p.Thr165=
XM_017011103.2:c.3465C>A	XP_016866592.1:p.Thr1155=
XM_017011104.1:c.3435C>A	XP_016866593.1:p.Thr1145=
XM_017011105.2:c.3405C>A	XP_016866594.1:p.Thr1135=
XM_017011106.2:c.3276C>A	XP_016866595.1:p.Thr1092=
XM_017011107.2:c.3255C>A	XP_016866596.1:p.Thr1085=
XR_002956289.1:n.3647C>A
NM_001363725.2:c.1104C>A	NP_001350654.1:p.Thr368=
NM_001371656.1:c.3483C>A	NP_001358585.1:p.Thr1161=
NM_001374820.1:c.3483C>A	NP_001361749.1:p.Thr1161=
NM_001374828.1:c.3603C>A MANE Select	NP_001361757.1:p.Thr1201=
NM_017519.3:c.3444C>A	NP_059989.3:p.Thr1148=