Canonical Allele Identifier: CA452781524

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510837A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189703A>G , CM000668.2:g.157189703A>G	GRCh38
NC_000006.11:g.157510837A>G , CM000668.1:g.157510837A>G	GRCh37
NC_000006.10:g.157552529A>G	NCBI36
NG_032093.1:g.416774A>G
NG_032093.2:g.416774A>G
NG_066624.1:g.418678A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3822A>G	ENSP00000055163.8:p.Ala1274=
ENST00000414678.8:c.3891A>G	ENSP00000412835.3:p.Ala1297=
ENST00000637015.2:c.4110A>G	ENSP00000489729.2:p.Ala1370=
ENST00000346085.10:c.3861A>G	ENSP00000344546.5:p.Ala1287=
ENST00000350026.10:c.3573A>G	ENSP00000055163.7:p.Ala1191=
ENST00000414678.7:c.2139A>G	ENSP00000412835.2:p.Ala713=
ENST00000635849.1:c.1302A>G	ENSP00000490948.1:p.Ala434=
ENST00000635957.1:c.936A>G	ENSP00000490385.1:p.Ala312=
ENST00000636930.2:c.3981A>G MANE Select	ENSP00000490491.2:p.Ala1327=
ENST00000636940.1:n.1978A>G
ENST00000637015.1:c.1349A>G
ENST00000637568.1:c.1263A>G
ENST00000637741.1:n.647A>G
ENST00000637810.1:c.1323A>G	ENSP00000489636.1:p.Ala441=
ENST00000637904.1:c.1482A>G	ENSP00000490550.1:p.Ala494=
ENST00000647938.1:c.3612A>G	ENSP00000498155.1:p.Ala1204=
ENST00000346085.9:c.3612A>G	ENSP00000344546.4:p.Ala1204=
ENST00000350026.9:c.3573A>G	ENSP00000055163.7:p.Ala1191=
ENST00000414678.6:c.2139A>G	ENSP00000412835.2:p.Ala713=
NM_017519.2:c.3573A>G	NP_059989.2:p.Ala1191=
NM_020732.3:c.3612A>G	NP_065783.3:p.Ala1204=
XM_005267069.3:c.3732A>G	XP_005267126.2:p.Ala1244=
XM_011535984.1:c.2811A>G	XP_011534286.1:p.Ala937=
XM_011535985.1:c.2631A>G	XP_011534287.1:p.Ala877=
XM_011535986.1:c.2391A>G	XP_011534288.1:p.Ala797=
XM_011535987.1:c.2010A>G	XP_011534289.1:p.Ala670=
XM_011535988.1:c.873A>G	XP_011534290.1:p.Ala291=
NM_001346813.1:c.3732A>G	NP_001333742.1:p.Ala1244=
NM_001363725.1:c.1482A>G	NP_001350654.1:p.Ala494=
XM_011535984.2:c.3942A>G	XP_011534286.2:p.Ala1314=
XM_011535988.3:c.873A>G	XP_011534290.1:p.Ala291=
XM_017011103.2:c.3843A>G	XP_016866592.1:p.Ala1281=
XM_017011104.1:c.3813A>G	XP_016866593.1:p.Ala1271=
XM_017011105.2:c.3783A>G	XP_016866594.1:p.Ala1261=
XM_017011106.2:c.3654A>G	XP_016866595.1:p.Ala1218=
XM_017011107.2:c.3633A>G	XP_016866596.1:p.Ala1211=
XR_002956289.1:n.4025A>G
NM_001363725.2:c.1482A>G	NP_001350654.1:p.Ala494=
NM_001371656.1:c.3861A>G	NP_001358585.1:p.Ala1287=
NM_001374820.1:c.3861A>G	NP_001361749.1:p.Ala1287=
NM_001374828.1:c.3981A>G MANE Select	NP_001361757.1:p.Ala1327=
NM_017519.3:c.3822A>G	NP_059989.3:p.Ala1274=