Canonical Allele Identifier: CA366234178

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510863C>G (hg19) ; chr6:g.157189729C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189729C>G , CM000668.2:g.157189729C>G	GRCh38
NC_000006.11:g.157510863C>G , CM000668.1:g.157510863C>G	GRCh37
NC_000006.10:g.157552555C>G	NCBI36
NG_032093.1:g.416800C>G
NG_032093.2:g.416800C>G
NG_066624.1:g.418704C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3848C>G	ENSP00000055163.8:p.Pro1283Arg
ENST00000414678.8:c.3917C>G	ENSP00000412835.3:p.Pro1306Arg
ENST00000637015.2:c.4136C>G	ENSP00000489729.2:p.Pro1379Arg
ENST00000346085.10:c.3887C>G	ENSP00000344546.5:p.Pro1296Arg
ENST00000350026.10:c.3599C>G	ENSP00000055163.7:p.Pro1200Arg
ENST00000414678.7:c.2165C>G	ENSP00000412835.2:p.Pro722Arg
ENST00000635849.1:c.1328C>G	ENSP00000490948.1:p.Pro443Arg
ENST00000635957.1:c.962C>G	ENSP00000490385.1:p.Pro321Arg
ENST00000636930.2:c.4007C>G MANE Select	ENSP00000490491.2:p.Pro1336Arg
ENST00000636940.1:n.2004C>G
ENST00000637015.1:c.1375C>G
ENST00000637568.1:c.1289C>G
ENST00000637741.1:n.673C>G
ENST00000637810.1:c.1349C>G	ENSP00000489636.1:p.Pro450Arg
ENST00000637904.1:c.1508C>G	ENSP00000490550.1:p.Pro503Arg
ENST00000647938.1:c.3638C>G	ENSP00000498155.1:p.Pro1213Arg
ENST00000346085.9:c.3638C>G	ENSP00000344546.4:p.Pro1213Arg
ENST00000350026.9:c.3599C>G	ENSP00000055163.7:p.Pro1200Arg
ENST00000414678.6:c.2165C>G	ENSP00000412835.2:p.Pro722Arg
NM_017519.2:c.3599C>G	NP_059989.2:p.Pro1200Arg
NM_020732.3:c.3638C>G	NP_065783.3:p.Pro1213Arg
XM_005267069.3:c.3758C>G	XP_005267126.2:p.Pro1253Arg
XM_011535984.1:c.2837C>G	XP_011534286.1:p.Pro946Arg
XM_011535985.1:c.2657C>G	XP_011534287.1:p.Pro886Arg
XM_011535986.1:c.2417C>G	XP_011534288.1:p.Pro806Arg
XM_011535987.1:c.2036C>G	XP_011534289.1:p.Pro679Arg
XM_011535988.1:c.899C>G	XP_011534290.1:p.Pro300Arg
NM_001346813.1:c.3758C>G	NP_001333742.1:p.Pro1253Arg
NM_001363725.1:c.1508C>G	NP_001350654.1:p.Pro503Arg
XM_011535984.2:c.3968C>G	XP_011534286.2:p.Pro1323Arg
XM_011535988.3:c.899C>G	XP_011534290.1:p.Pro300Arg
XM_017011103.2:c.3869C>G	XP_016866592.1:p.Pro1290Arg
XM_017011104.1:c.3839C>G	XP_016866593.1:p.Pro1280Arg
XM_017011105.2:c.3809C>G	XP_016866594.1:p.Pro1270Arg
XM_017011106.2:c.3680C>G	XP_016866595.1:p.Pro1227Arg
XM_017011107.2:c.3659C>G	XP_016866596.1:p.Pro1220Arg
XR_002956289.1:n.4051C>G
NM_001363725.2:c.1508C>G	NP_001350654.1:p.Pro503Arg
NM_001371656.1:c.3887C>G	NP_001358585.1:p.Pro1296Arg
NM_001374820.1:c.3887C>G	NP_001361749.1:p.Pro1296Arg
NM_001374828.1:c.4007C>G MANE Select	NP_001361757.1:p.Pro1336Arg
NM_017519.3:c.3848C>G	NP_059989.3:p.Pro1283Arg