Canonical Allele Identifier: CA452781549

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510867C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189733C>A , CM000668.2:g.157189733C>A	GRCh38
NC_000006.11:g.157510867C>A , CM000668.1:g.157510867C>A	GRCh37
NC_000006.10:g.157552559C>A	NCBI36
NG_032093.1:g.416804C>A
NG_032093.2:g.416804C>A
NG_066624.1:g.418708C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3852C>A	ENSP00000055163.8:p.Thr1284=
ENST00000414678.8:c.3921C>A	ENSP00000412835.3:p.Thr1307=
ENST00000637015.2:c.4140C>A	ENSP00000489729.2:p.Thr1380=
ENST00000346085.10:c.3891C>A	ENSP00000344546.5:p.Thr1297=
ENST00000350026.10:c.3603C>A	ENSP00000055163.7:p.Thr1201=
ENST00000414678.7:c.2169C>A	ENSP00000412835.2:p.Thr723=
ENST00000635849.1:c.1332C>A	ENSP00000490948.1:p.Thr444=
ENST00000635957.1:c.966C>A	ENSP00000490385.1:p.Thr322=
ENST00000636930.2:c.4011C>A MANE Select	ENSP00000490491.2:p.Thr1337=
ENST00000636940.1:n.2008C>A
ENST00000637015.1:c.1379C>A
ENST00000637568.1:c.1293C>A
ENST00000637741.1:n.677C>A
ENST00000637810.1:c.1353C>A	ENSP00000489636.1:p.Thr451=
ENST00000637904.1:c.1512C>A	ENSP00000490550.1:p.Thr504=
ENST00000647938.1:c.3642C>A	ENSP00000498155.1:p.Thr1214=
ENST00000346085.9:c.3642C>A	ENSP00000344546.4:p.Thr1214=
ENST00000350026.9:c.3603C>A	ENSP00000055163.7:p.Thr1201=
ENST00000414678.6:c.2169C>A	ENSP00000412835.2:p.Thr723=
NM_017519.2:c.3603C>A	NP_059989.2:p.Thr1201=
NM_020732.3:c.3642C>A	NP_065783.3:p.Thr1214=
XM_005267069.3:c.3762C>A	XP_005267126.2:p.Thr1254=
XM_011535984.1:c.2841C>A	XP_011534286.1:p.Thr947=
XM_011535985.1:c.2661C>A	XP_011534287.1:p.Thr887=
XM_011535986.1:c.2421C>A	XP_011534288.1:p.Thr807=
XM_011535987.1:c.2040C>A	XP_011534289.1:p.Thr680=
XM_011535988.1:c.903C>A	XP_011534290.1:p.Thr301=
NM_001346813.1:c.3762C>A	NP_001333742.1:p.Thr1254=
NM_001363725.1:c.1512C>A	NP_001350654.1:p.Thr504=
XM_011535984.2:c.3972C>A	XP_011534286.2:p.Thr1324=
XM_011535988.3:c.903C>A	XP_011534290.1:p.Thr301=
XM_017011103.2:c.3873C>A	XP_016866592.1:p.Thr1291=
XM_017011104.1:c.3843C>A	XP_016866593.1:p.Thr1281=
XM_017011105.2:c.3813C>A	XP_016866594.1:p.Thr1271=
XM_017011106.2:c.3684C>A	XP_016866595.1:p.Thr1228=
XM_017011107.2:c.3663C>A	XP_016866596.1:p.Thr1221=
XR_002956289.1:n.4055C>A
NM_001363725.2:c.1512C>A	NP_001350654.1:p.Thr504=
NM_001371656.1:c.3891C>A	NP_001358585.1:p.Thr1297=
NM_001374820.1:c.3891C>A	NP_001361749.1:p.Thr1297=
NM_001374828.1:c.4011C>A MANE Select	NP_001361757.1:p.Thr1337=
NM_017519.3:c.3852C>A	NP_059989.3:p.Thr1284=