Canonical Allele Identifier: CA452781490

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510783G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189649G>T , CM000668.2:g.157189649G>T	GRCh38
NC_000006.11:g.157510783G>T , CM000668.1:g.157510783G>T	GRCh37
NC_000006.10:g.157552475G>T	NCBI36
NG_032093.1:g.416720G>T
NG_032093.2:g.416720G>T
NG_066624.1:g.418624G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3768G>T	ENSP00000055163.8:p.Ser1256=
ENST00000414678.8:c.3837G>T	ENSP00000412835.3:p.Ser1279=
ENST00000637015.2:c.4056G>T	ENSP00000489729.2:p.Ser1352=
ENST00000346085.10:c.3807G>T	ENSP00000344546.5:p.Ser1269=
ENST00000350026.10:c.3519G>T	ENSP00000055163.7:p.Ser1173=
ENST00000414678.7:c.2085G>T	ENSP00000412835.2:p.Ser695=
ENST00000635849.1:c.1248G>T	ENSP00000490948.1:p.Ser416=
ENST00000635957.1:c.882G>T	ENSP00000490385.1:p.Ser294=
ENST00000636930.2:c.3927G>T MANE Select	ENSP00000490491.2:p.Ser1309=
ENST00000636940.1:n.1924G>T
ENST00000637015.1:c.1295G>T
ENST00000637568.1:c.1209G>T
ENST00000637741.1:n.593G>T
ENST00000637810.1:c.1269G>T	ENSP00000489636.1:p.Ser423=
ENST00000637904.1:c.1428G>T	ENSP00000490550.1:p.Ser476=
ENST00000647938.1:c.3558G>T	ENSP00000498155.1:p.Ser1186=
ENST00000346085.9:c.3558G>T	ENSP00000344546.4:p.Ser1186=
ENST00000350026.9:c.3519G>T	ENSP00000055163.7:p.Ser1173=
ENST00000414678.6:c.2085G>T	ENSP00000412835.2:p.Ser695=
NM_017519.2:c.3519G>T	NP_059989.2:p.Ser1173=
NM_020732.3:c.3558G>T	NP_065783.3:p.Ser1186=
XM_005267069.3:c.3678G>T	XP_005267126.2:p.Ser1226=
XM_011535984.1:c.2757G>T	XP_011534286.1:p.Ser919=
XM_011535985.1:c.2577G>T	XP_011534287.1:p.Ser859=
XM_011535986.1:c.2337G>T	XP_011534288.1:p.Ser779=
XM_011535987.1:c.1956G>T	XP_011534289.1:p.Ser652=
XM_011535988.1:c.819G>T	XP_011534290.1:p.Ser273=
NM_001346813.1:c.3678G>T	NP_001333742.1:p.Ser1226=
NM_001363725.1:c.1428G>T	NP_001350654.1:p.Ser476=
XM_011535984.2:c.3888G>T	XP_011534286.2:p.Ser1296=
XM_011535988.3:c.819G>T	XP_011534290.1:p.Ser273=
XM_017011103.2:c.3789G>T	XP_016866592.1:p.Ser1263=
XM_017011104.1:c.3759G>T	XP_016866593.1:p.Ser1253=
XM_017011105.2:c.3729G>T	XP_016866594.1:p.Ser1243=
XM_017011106.2:c.3600G>T	XP_016866595.1:p.Ser1200=
XM_017011107.2:c.3579G>T	XP_016866596.1:p.Ser1193=
XR_002956289.1:n.3971G>T
NM_001363725.2:c.1428G>T	NP_001350654.1:p.Ser476=
NM_001371656.1:c.3807G>T	NP_001358585.1:p.Ser1269=
NM_001374820.1:c.3807G>T	NP_001361749.1:p.Ser1269=
NM_001374828.1:c.3927G>T MANE Select	NP_001361757.1:p.Ser1309=
NM_017519.3:c.3768G>T	NP_059989.3:p.Ser1256=