Canonical Allele Identifier: CA2713234762

Gene: ARID1B

Linked Data

• dbSNP Id: rs1792506929

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181229C>A , CM000668.2:g.157181229C>A	GRCh38
NC_000006.11:g.157502363C>A , CM000668.1:g.157502363C>A	GRCh37
NC_000006.10:g.157544055C>A	NCBI36
NG_032093.1:g.408300C>A
NG_032093.2:g.408300C>A
NG_066624.1:g.410204C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3555+51C>A	ENSP00000055163.8:n.3555+51C>A
ENST00000414678.8:c.3624+51C>A	ENSP00000412835.3:n.3624+51C>A
ENST00000637015.2:c.3843+51C>A	ENSP00000489729.2:n.3843+51C>A
ENST00000319584.11:c.1728+51C>A	ENSP00000313006.7:n.1728+51C>A
ENST00000346085.10:c.3594+51C>A	ENSP00000344546.5:n.3594+51C>A
ENST00000350026.10:c.3306+51C>A	ENSP00000055163.7:n.3306+51C>A
ENST00000414678.7:c.1872+51C>A	ENSP00000412835.2:n.1872+51C>A
ENST00000635849.1:c.1035+51C>A	ENSP00000490948.1:n.1035+51C>A
ENST00000635957.1:c.669+51C>A	ENSP00000490385.1:n.669+51C>A
ENST00000636930.2:c.3714+51C>A MANE Select	ENSP00000490491.2:n.3714+51C>A
ENST00000636940.1:n.1711+51C>A
ENST00000637015.1:c.1082+51C>A
ENST00000637568.1:c.996+51C>A
ENST00000637741.1:n.380+51C>A
ENST00000637810.1:c.1056+51C>A	ENSP00000489636.1:n.1056+51C>A
ENST00000637904.1:c.1215+51C>A	ENSP00000490550.1:n.1215+51C>A
ENST00000647938.1:c.3345+51C>A	ENSP00000498155.1:n.3345+51C>A
ENST00000319584.10:c.1731+51C>A	ENSP00000313006.6:n.1731+51C>A
ENST00000346085.9:c.3345+51C>A	ENSP00000344546.4:n.3345+51C>A
ENST00000350026.9:c.3306+51C>A	ENSP00000055163.7:n.3306+51C>A
ENST00000400790.3:c.507+51C>A	ENSP00000383596.3:n.507+51C>A
ENST00000414678.6:c.1872+51C>A	ENSP00000412835.2:n.1872+51C>A
NM_017519.2:c.3306+51C>A	NP_059989.2:n.3306+51C>A
NM_020732.3:c.3345+51C>A	NP_065783.3:n.3345+51C>A
XM_005267069.3:c.3465+51C>A	XP_005267126.2:n.3465+51C>A
XM_011535984.1:c.2544+51C>A	XP_011534286.1:n.2544+51C>A
XM_011535985.1:c.2364+51C>A	XP_011534287.1:n.2364+51C>A
XM_011535986.1:c.2124+51C>A	XP_011534288.1:n.2124+51C>A
XM_011535987.1:c.1743+51C>A	XP_011534289.1:n.1743+51C>A
XM_011535988.1:c.606+51C>A	XP_011534290.1:n.606+51C>A
NM_001346813.1:c.3465+51C>A	NP_001333742.1:n.3465+51C>A
NM_001363725.1:c.1215+51C>A	NP_001350654.1:n.1215+51C>A
XM_011535984.2:c.3675+51C>A	XP_011534286.2:n.3675+51C>A
XM_011535988.3:c.606+51C>A	XP_011534290.1:n.606+51C>A
XM_017011103.2:c.3576+51C>A	XP_016866592.1:n.3576+51C>A
XM_017011104.1:c.3546+51C>A	XP_016866593.1:n.3546+51C>A
XM_017011105.2:c.3516+51C>A	XP_016866594.1:n.3516+51C>A
XM_017011106.2:c.3387+51C>A	XP_016866595.1:n.3387+51C>A
XM_017011107.2:c.3366+51C>A	XP_016866596.1:n.3366+51C>A
XR_002956289.1:n.3758+51C>A
NM_001363725.2:c.1215+51C>A	NP_001350654.1:n.1215+51C>A
NM_001371656.1:c.3594+51C>A	NP_001358585.1:n.3594+51C>A
NM_001374820.1:c.3594+51C>A	NP_001361749.1:n.3594+51C>A
NM_001374828.1:c.3714+51C>A MANE Select	NP_001361757.1:n.3714+51C>A
NM_017519.3:c.3555+51C>A	NP_059989.3:n.3555+51C>A