Canonical Allele Identifier: CA366234278

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510894G>T (hg19) ; chr6:g.157189760G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189760G>T , CM000668.2:g.157189760G>T	GRCh38
NC_000006.11:g.157510894G>T , CM000668.1:g.157510894G>T	GRCh37
NC_000006.10:g.157552586G>T	NCBI36
NG_032093.1:g.416831G>T
NG_032093.2:g.416831G>T
NG_066624.1:g.418735G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3879G>T	ENSP00000055163.8:p.Met1293Ile
ENST00000414678.8:c.3948G>T	ENSP00000412835.3:p.Met1316Ile
ENST00000637015.2:c.4167G>T	ENSP00000489729.2:p.Met1389Ile
ENST00000346085.10:c.3918G>T	ENSP00000344546.5:p.Met1306Ile
ENST00000350026.10:c.3630G>T	ENSP00000055163.7:p.Met1210Ile
ENST00000414678.7:c.2196G>T	ENSP00000412835.2:p.Met732Ile
ENST00000635849.1:c.1359G>T	ENSP00000490948.1:p.Met453Ile
ENST00000635957.1:c.993G>T	ENSP00000490385.1:p.Met331Ile
ENST00000636930.2:c.4038G>T MANE Select	ENSP00000490491.2:p.Met1346Ile
ENST00000636940.1:n.2035G>T
ENST00000637015.1:c.1406G>T
ENST00000637568.1:c.1320G>T
ENST00000637741.1:n.704G>T
ENST00000637810.1:c.1380G>T	ENSP00000489636.1:p.Met460Ile
ENST00000637904.1:c.1539G>T	ENSP00000490550.1:p.Met513Ile
ENST00000647938.1:c.3669G>T	ENSP00000498155.1:p.Met1223Ile
ENST00000346085.9:c.3669G>T	ENSP00000344546.4:p.Met1223Ile
ENST00000350026.9:c.3630G>T	ENSP00000055163.7:p.Met1210Ile
ENST00000414678.6:c.2196G>T	ENSP00000412835.2:p.Met732Ile
NM_017519.2:c.3630G>T	NP_059989.2:p.Met1210Ile
NM_020732.3:c.3669G>T	NP_065783.3:p.Met1223Ile
XM_005267069.3:c.3789G>T	XP_005267126.2:p.Met1263Ile
XM_011535984.1:c.2868G>T	XP_011534286.1:p.Met956Ile
XM_011535985.1:c.2688G>T	XP_011534287.1:p.Met896Ile
XM_011535986.1:c.2448G>T	XP_011534288.1:p.Met816Ile
XM_011535987.1:c.2067G>T	XP_011534289.1:p.Met689Ile
XM_011535988.1:c.930G>T	XP_011534290.1:p.Met310Ile
NM_001346813.1:c.3789G>T	NP_001333742.1:p.Met1263Ile
NM_001363725.1:c.1539G>T	NP_001350654.1:p.Met513Ile
XM_011535984.2:c.3999G>T	XP_011534286.2:p.Met1333Ile
XM_011535988.3:c.930G>T	XP_011534290.1:p.Met310Ile
XM_017011103.2:c.3900G>T	XP_016866592.1:p.Met1300Ile
XM_017011104.1:c.3870G>T	XP_016866593.1:p.Met1290Ile
XM_017011105.2:c.3840G>T	XP_016866594.1:p.Met1280Ile
XM_017011106.2:c.3711G>T	XP_016866595.1:p.Met1237Ile
XM_017011107.2:c.3690G>T	XP_016866596.1:p.Met1230Ile
XR_002956289.1:n.4082G>T
NM_001363725.2:c.1539G>T	NP_001350654.1:p.Met513Ile
NM_001371656.1:c.3918G>T	NP_001358585.1:p.Met1306Ile
NM_001374820.1:c.3918G>T	NP_001361749.1:p.Met1306Ile
NM_001374828.1:c.4038G>T MANE Select	NP_001361757.1:p.Met1346Ile
NM_017519.3:c.3879G>T	NP_059989.3:p.Met1293Ile