Canonical Allele Identifier: CA452781521

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510831C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189697C>A , CM000668.2:g.157189697C>A	GRCh38
NC_000006.11:g.157510831C>A , CM000668.1:g.157510831C>A	GRCh37
NC_000006.10:g.157552523C>A	NCBI36
NG_032093.1:g.416768C>A
NG_032093.2:g.416768C>A
NG_066624.1:g.418672C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3816C>A	ENSP00000055163.8:p.Ser1272=
ENST00000414678.8:c.3885C>A	ENSP00000412835.3:p.Ser1295=
ENST00000637015.2:c.4104C>A	ENSP00000489729.2:p.Ser1368=
ENST00000346085.10:c.3855C>A	ENSP00000344546.5:p.Ser1285=
ENST00000350026.10:c.3567C>A	ENSP00000055163.7:p.Ser1189=
ENST00000414678.7:c.2133C>A	ENSP00000412835.2:p.Ser711=
ENST00000635849.1:c.1296C>A	ENSP00000490948.1:p.Ser432=
ENST00000635957.1:c.930C>A	ENSP00000490385.1:p.Ser310=
ENST00000636930.2:c.3975C>A MANE Select	ENSP00000490491.2:p.Ser1325=
ENST00000636940.1:n.1972C>A
ENST00000637015.1:c.1343C>A
ENST00000637568.1:c.1257C>A
ENST00000637741.1:n.641C>A
ENST00000637810.1:c.1317C>A	ENSP00000489636.1:p.Ser439=
ENST00000637904.1:c.1476C>A	ENSP00000490550.1:p.Ser492=
ENST00000647938.1:c.3606C>A	ENSP00000498155.1:p.Ser1202=
ENST00000346085.9:c.3606C>A	ENSP00000344546.4:p.Ser1202=
ENST00000350026.9:c.3567C>A	ENSP00000055163.7:p.Ser1189=
ENST00000414678.6:c.2133C>A	ENSP00000412835.2:p.Ser711=
NM_017519.2:c.3567C>A	NP_059989.2:p.Ser1189=
NM_020732.3:c.3606C>A	NP_065783.3:p.Ser1202=
XM_005267069.3:c.3726C>A	XP_005267126.2:p.Ser1242=
XM_011535984.1:c.2805C>A	XP_011534286.1:p.Ser935=
XM_011535985.1:c.2625C>A	XP_011534287.1:p.Ser875=
XM_011535986.1:c.2385C>A	XP_011534288.1:p.Ser795=
XM_011535987.1:c.2004C>A	XP_011534289.1:p.Ser668=
XM_011535988.1:c.867C>A	XP_011534290.1:p.Ser289=
NM_001346813.1:c.3726C>A	NP_001333742.1:p.Ser1242=
NM_001363725.1:c.1476C>A	NP_001350654.1:p.Ser492=
XM_011535984.2:c.3936C>A	XP_011534286.2:p.Ser1312=
XM_011535988.3:c.867C>A	XP_011534290.1:p.Ser289=
XM_017011103.2:c.3837C>A	XP_016866592.1:p.Ser1279=
XM_017011104.1:c.3807C>A	XP_016866593.1:p.Ser1269=
XM_017011105.2:c.3777C>A	XP_016866594.1:p.Ser1259=
XM_017011106.2:c.3648C>A	XP_016866595.1:p.Ser1216=
XM_017011107.2:c.3627C>A	XP_016866596.1:p.Ser1209=
XR_002956289.1:n.4019C>A
NM_001363725.2:c.1476C>A	NP_001350654.1:p.Ser492=
NM_001371656.1:c.3855C>A	NP_001358585.1:p.Ser1285=
NM_001374820.1:c.3855C>A	NP_001361749.1:p.Ser1285=
NM_001374828.1:c.3975C>A MANE Select	NP_001361757.1:p.Ser1325=
NM_017519.3:c.3816C>A	NP_059989.3:p.Ser1272=