Canonical Allele Identifier: CA452781547

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510864T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189730T>G , CM000668.2:g.157189730T>G	GRCh38
NC_000006.11:g.157510864T>G , CM000668.1:g.157510864T>G	GRCh37
NC_000006.10:g.157552556T>G	NCBI36
NG_032093.1:g.416801T>G
NG_032093.2:g.416801T>G
NG_066624.1:g.418705T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3849T>G	ENSP00000055163.8:p.Pro1283=
ENST00000414678.8:c.3918T>G	ENSP00000412835.3:p.Pro1306=
ENST00000637015.2:c.4137T>G	ENSP00000489729.2:p.Pro1379=
ENST00000346085.10:c.3888T>G	ENSP00000344546.5:p.Pro1296=
ENST00000350026.10:c.3600T>G	ENSP00000055163.7:p.Pro1200=
ENST00000414678.7:c.2166T>G	ENSP00000412835.2:p.Pro722=
ENST00000635849.1:c.1329T>G	ENSP00000490948.1:p.Pro443=
ENST00000635957.1:c.963T>G	ENSP00000490385.1:p.Pro321=
ENST00000636930.2:c.4008T>G MANE Select	ENSP00000490491.2:p.Pro1336=
ENST00000636940.1:n.2005T>G
ENST00000637015.1:c.1376T>G
ENST00000637568.1:c.1290T>G
ENST00000637741.1:n.674T>G
ENST00000637810.1:c.1350T>G	ENSP00000489636.1:p.Pro450=
ENST00000637904.1:c.1509T>G	ENSP00000490550.1:p.Pro503=
ENST00000647938.1:c.3639T>G	ENSP00000498155.1:p.Pro1213=
ENST00000346085.9:c.3639T>G	ENSP00000344546.4:p.Pro1213=
ENST00000350026.9:c.3600T>G	ENSP00000055163.7:p.Pro1200=
ENST00000414678.6:c.2166T>G	ENSP00000412835.2:p.Pro722=
NM_017519.2:c.3600T>G	NP_059989.2:p.Pro1200=
NM_020732.3:c.3639T>G	NP_065783.3:p.Pro1213=
XM_005267069.3:c.3759T>G	XP_005267126.2:p.Pro1253=
XM_011535984.1:c.2838T>G	XP_011534286.1:p.Pro946=
XM_011535985.1:c.2658T>G	XP_011534287.1:p.Pro886=
XM_011535986.1:c.2418T>G	XP_011534288.1:p.Pro806=
XM_011535987.1:c.2037T>G	XP_011534289.1:p.Pro679=
XM_011535988.1:c.900T>G	XP_011534290.1:p.Pro300=
NM_001346813.1:c.3759T>G	NP_001333742.1:p.Pro1253=
NM_001363725.1:c.1509T>G	NP_001350654.1:p.Pro503=
XM_011535984.2:c.3969T>G	XP_011534286.2:p.Pro1323=
XM_011535988.3:c.900T>G	XP_011534290.1:p.Pro300=
XM_017011103.2:c.3870T>G	XP_016866592.1:p.Pro1290=
XM_017011104.1:c.3840T>G	XP_016866593.1:p.Pro1280=
XM_017011105.2:c.3810T>G	XP_016866594.1:p.Pro1270=
XM_017011106.2:c.3681T>G	XP_016866595.1:p.Pro1227=
XM_017011107.2:c.3660T>G	XP_016866596.1:p.Pro1220=
XR_002956289.1:n.4052T>G
NM_001363725.2:c.1509T>G	NP_001350654.1:p.Pro503=
NM_001371656.1:c.3888T>G	NP_001358585.1:p.Pro1296=
NM_001374820.1:c.3888T>G	NP_001361749.1:p.Pro1296=
NM_001374828.1:c.4008T>G MANE Select	NP_001361757.1:p.Pro1336=
NM_017519.3:c.3849T>G	NP_059989.3:p.Pro1283=