Canonical Allele Identifier: CA2713416038

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128318247

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181233C>G , CM000668.2:g.157181233C>G	GRCh38
NC_000006.11:g.157502367C>G , CM000668.1:g.157502367C>G	GRCh37
NC_000006.10:g.157544059C>G	NCBI36
NG_032093.1:g.408304C>G
NG_032093.2:g.408304C>G
NG_066624.1:g.410208C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3555+55C>G	ENSP00000055163.8:n.3555+55C>G
ENST00000414678.8:c.3624+55C>G	ENSP00000412835.3:n.3624+55C>G
ENST00000637015.2:c.3843+55C>G	ENSP00000489729.2:n.3843+55C>G
ENST00000319584.11:c.1728+55C>G	ENSP00000313006.7:n.1728+55C>G
ENST00000346085.10:c.3594+55C>G	ENSP00000344546.5:n.3594+55C>G
ENST00000350026.10:c.3306+55C>G	ENSP00000055163.7:n.3306+55C>G
ENST00000414678.7:c.1872+55C>G	ENSP00000412835.2:n.1872+55C>G
ENST00000635849.1:c.1035+55C>G	ENSP00000490948.1:n.1035+55C>G
ENST00000635957.1:c.669+55C>G	ENSP00000490385.1:n.669+55C>G
ENST00000636930.2:c.3714+55C>G MANE Select	ENSP00000490491.2:n.3714+55C>G
ENST00000636940.1:n.1711+55C>G
ENST00000637015.1:c.1082+55C>G
ENST00000637568.1:c.996+55C>G
ENST00000637741.1:n.380+55C>G
ENST00000637810.1:c.1056+55C>G	ENSP00000489636.1:n.1056+55C>G
ENST00000637904.1:c.1215+55C>G	ENSP00000490550.1:n.1215+55C>G
ENST00000647938.1:c.3345+55C>G	ENSP00000498155.1:n.3345+55C>G
ENST00000319584.10:c.1731+55C>G	ENSP00000313006.6:n.1731+55C>G
ENST00000346085.9:c.3345+55C>G	ENSP00000344546.4:n.3345+55C>G
ENST00000350026.9:c.3306+55C>G	ENSP00000055163.7:n.3306+55C>G
ENST00000400790.3:c.507+55C>G	ENSP00000383596.3:n.507+55C>G
ENST00000414678.6:c.1872+55C>G	ENSP00000412835.2:n.1872+55C>G
NM_017519.2:c.3306+55C>G	NP_059989.2:n.3306+55C>G
NM_020732.3:c.3345+55C>G	NP_065783.3:n.3345+55C>G
XM_005267069.3:c.3465+55C>G	XP_005267126.2:n.3465+55C>G
XM_011535984.1:c.2544+55C>G	XP_011534286.1:n.2544+55C>G
XM_011535985.1:c.2364+55C>G	XP_011534287.1:n.2364+55C>G
XM_011535986.1:c.2124+55C>G	XP_011534288.1:n.2124+55C>G
XM_011535987.1:c.1743+55C>G	XP_011534289.1:n.1743+55C>G
XM_011535988.1:c.606+55C>G	XP_011534290.1:n.606+55C>G
NM_001346813.1:c.3465+55C>G	NP_001333742.1:n.3465+55C>G
NM_001363725.1:c.1215+55C>G	NP_001350654.1:n.1215+55C>G
XM_011535984.2:c.3675+55C>G	XP_011534286.2:n.3675+55C>G
XM_011535988.3:c.606+55C>G	XP_011534290.1:n.606+55C>G
XM_017011103.2:c.3576+55C>G	XP_016866592.1:n.3576+55C>G
XM_017011104.1:c.3546+55C>G	XP_016866593.1:n.3546+55C>G
XM_017011105.2:c.3516+55C>G	XP_016866594.1:n.3516+55C>G
XM_017011106.2:c.3387+55C>G	XP_016866595.1:n.3387+55C>G
XM_017011107.2:c.3366+55C>G	XP_016866596.1:n.3366+55C>G
XR_002956289.1:n.3758+55C>G
NM_001363725.2:c.1215+55C>G	NP_001350654.1:n.1215+55C>G
NM_001371656.1:c.3594+55C>G	NP_001358585.1:n.3594+55C>G
NM_001374820.1:c.3594+55C>G	NP_001361749.1:n.3594+55C>G
NM_001374828.1:c.3714+55C>G MANE Select	NP_001361757.1:n.3714+55C>G
NM_017519.3:c.3555+55C>G	NP_059989.3:n.3555+55C>G