Canonical Allele Identifier: CA452781920

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511259C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190125C>T , CM000668.2:g.157190125C>T	GRCh38
NC_000006.11:g.157511259C>T , CM000668.1:g.157511259C>T	GRCh37
NC_000006.10:g.157552951C>T	NCBI36
NG_032093.1:g.417196C>T
NG_032093.2:g.417196C>T
NG_066624.1:g.419100C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3987C>T	ENSP00000055163.8:p.Pro1329=
ENST00000414678.8:c.4056C>T	ENSP00000412835.3:p.Pro1352=
ENST00000637015.2:c.4275C>T	ENSP00000489729.2:p.Pro1425=
ENST00000346085.10:c.4026C>T	ENSP00000344546.5:p.Pro1342=
ENST00000350026.10:c.3738C>T	ENSP00000055163.7:p.Pro1246=
ENST00000414678.7:c.2304C>T	ENSP00000412835.2:p.Pro768=
ENST00000635849.1:c.1467C>T	ENSP00000490948.1:p.Pro489=
ENST00000635957.1:c.1098C>T	ENSP00000490385.1:p.Pro366=
ENST00000636930.2:c.4146C>T MANE Select	ENSP00000490491.2:p.Pro1382=
ENST00000636940.1:n.2143C>T
ENST00000637015.1:c.1514C>T
ENST00000637568.1:c.1428C>T
ENST00000637741.1:n.812C>T
ENST00000637810.1:c.1488C>T	ENSP00000489636.1:p.Pro496=
ENST00000637904.1:c.1647C>T	ENSP00000490550.1:p.Pro549=
ENST00000647938.1:c.3777C>T	ENSP00000498155.1:p.Pro1259=
ENST00000346085.9:c.3777C>T	ENSP00000344546.4:p.Pro1259=
ENST00000350026.9:c.3738C>T	ENSP00000055163.7:p.Pro1246=
ENST00000414678.6:c.2304C>T	ENSP00000412835.2:p.Pro768=
NM_017519.2:c.3738C>T	NP_059989.2:p.Pro1246=
NM_020732.3:c.3777C>T	NP_065783.3:p.Pro1259=
XM_005267069.3:c.3897C>T	XP_005267126.2:p.Pro1299=
XM_011535984.1:c.2976C>T	XP_011534286.1:p.Pro992=
XM_011535985.1:c.2796C>T	XP_011534287.1:p.Pro932=
XM_011535986.1:c.2556C>T	XP_011534288.1:p.Pro852=
XM_011535987.1:c.2175C>T	XP_011534289.1:p.Pro725=
XM_011535988.1:c.1038C>T	XP_011534290.1:p.Pro346=
NM_001346813.1:c.3897C>T	NP_001333742.1:p.Pro1299=
NM_001363725.1:c.1647C>T	NP_001350654.1:p.Pro549=
XM_011535984.2:c.4107C>T	XP_011534286.2:p.Pro1369=
XM_011535988.3:c.1038C>T	XP_011534290.1:p.Pro346=
XM_017011103.2:c.4008C>T	XP_016866592.1:p.Pro1336=
XM_017011104.1:c.3978C>T	XP_016866593.1:p.Pro1326=
XM_017011105.2:c.3948C>T	XP_016866594.1:p.Pro1316=
XM_017011106.2:c.3819C>T	XP_016866595.1:p.Pro1273=
XM_017011107.2:c.3798C>T	XP_016866596.1:p.Pro1266=
XR_002956289.1:n.4190C>T
NM_001363725.2:c.1647C>T	NP_001350654.1:p.Pro549=
NM_001371656.1:c.4026C>T	NP_001358585.1:p.Pro1342=
NM_001374820.1:c.4026C>T	NP_001361749.1:p.Pro1342=
NM_001374828.1:c.4146C>T MANE Select	NP_001361757.1:p.Pro1382=
NM_017519.3:c.3987C>T	NP_059989.3:p.Pro1329=