Canonical Allele Identifier: CA366235028

Gene: ARID1B

Linked Data

• COSMIC: COSM309265 ; COSM5659699
• MyVariant Identifiers: chr6:g.157511215G>T (hg19) ; chr6:g.157190081G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190081G>T , CM000668.2:g.157190081G>T	GRCh38
NC_000006.11:g.157511215G>T , CM000668.1:g.157511215G>T	GRCh37
NC_000006.10:g.157552907G>T	NCBI36
NG_032093.1:g.417152G>T
NG_032093.2:g.417152G>T
NG_066624.1:g.419056G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3943G>T	ENSP00000055163.8:p.Asp1315Tyr
ENST00000414678.8:c.4012G>T	ENSP00000412835.3:p.Asp1338Tyr
ENST00000637015.2:c.4231G>T	ENSP00000489729.2:p.Asp1411Tyr
ENST00000346085.10:c.3982G>T	ENSP00000344546.5:p.Asp1328Tyr
ENST00000350026.10:c.3694G>T	ENSP00000055163.7:p.Asp1232Tyr
ENST00000414678.7:c.2260G>T	ENSP00000412835.2:p.Asp754Tyr
ENST00000635849.1:c.1423G>T	ENSP00000490948.1:p.Asp475Tyr
ENST00000635957.1:c.1054G>T	ENSP00000490385.1:p.Asp352Tyr
ENST00000636930.2:c.4102G>T MANE Select	ENSP00000490491.2:p.Asp1368Tyr
ENST00000636940.1:n.2099G>T
ENST00000637015.1:c.1470G>T
ENST00000637568.1:c.1384G>T
ENST00000637741.1:n.768G>T
ENST00000637810.1:c.1444G>T	ENSP00000489636.1:p.Asp482Tyr
ENST00000637904.1:c.1603G>T	ENSP00000490550.1:p.Asp535Tyr
ENST00000647938.1:c.3733G>T	ENSP00000498155.1:p.Asp1245Tyr
ENST00000346085.9:c.3733G>T	ENSP00000344546.4:p.Asp1245Tyr
ENST00000350026.9:c.3694G>T	ENSP00000055163.7:p.Asp1232Tyr
ENST00000414678.6:c.2260G>T	ENSP00000412835.2:p.Asp754Tyr
NM_017519.2:c.3694G>T	NP_059989.2:p.Asp1232Tyr
NM_020732.3:c.3733G>T	NP_065783.3:p.Asp1245Tyr
XM_005267069.3:c.3853G>T	XP_005267126.2:p.Asp1285Tyr
XM_011535984.1:c.2932G>T	XP_011534286.1:p.Asp978Tyr
XM_011535985.1:c.2752G>T	XP_011534287.1:p.Asp918Tyr
XM_011535986.1:c.2512G>T	XP_011534288.1:p.Asp838Tyr
XM_011535987.1:c.2131G>T	XP_011534289.1:p.Asp711Tyr
XM_011535988.1:c.994G>T	XP_011534290.1:p.Asp332Tyr
NM_001346813.1:c.3853G>T	NP_001333742.1:p.Asp1285Tyr
NM_001363725.1:c.1603G>T	NP_001350654.1:p.Asp535Tyr
XM_011535984.2:c.4063G>T	XP_011534286.2:p.Asp1355Tyr
XM_011535988.3:c.994G>T	XP_011534290.1:p.Asp332Tyr
XM_017011103.2:c.3964G>T	XP_016866592.1:p.Asp1322Tyr
XM_017011104.1:c.3934G>T	XP_016866593.1:p.Asp1312Tyr
XM_017011105.2:c.3904G>T	XP_016866594.1:p.Asp1302Tyr
XM_017011106.2:c.3775G>T	XP_016866595.1:p.Asp1259Tyr
XM_017011107.2:c.3754G>T	XP_016866596.1:p.Asp1252Tyr
XR_002956289.1:n.4146G>T
NM_001363725.2:c.1603G>T	NP_001350654.1:p.Asp535Tyr
NM_001371656.1:c.3982G>T	NP_001358585.1:p.Asp1328Tyr
NM_001374820.1:c.3982G>T	NP_001361749.1:p.Asp1328Tyr
NM_001374828.1:c.4102G>T MANE Select	NP_001361757.1:p.Asp1368Tyr
NM_017519.3:c.3943G>T	NP_059989.3:p.Asp1315Tyr