Canonical Allele Identifier: CA452781542

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510858G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189724G>A , CM000668.2:g.157189724G>A	GRCh38
NC_000006.11:g.157510858G>A , CM000668.1:g.157510858G>A	GRCh37
NC_000006.10:g.157552550G>A	NCBI36
NG_032093.1:g.416795G>A
NG_032093.2:g.416795G>A
NG_066624.1:g.418699G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3843G>A	ENSP00000055163.8:p.Lys1281=
ENST00000414678.8:c.3912G>A	ENSP00000412835.3:p.Lys1304=
ENST00000637015.2:c.4131G>A	ENSP00000489729.2:p.Lys1377=
ENST00000346085.10:c.3882G>A	ENSP00000344546.5:p.Lys1294=
ENST00000350026.10:c.3594G>A	ENSP00000055163.7:p.Lys1198=
ENST00000414678.7:c.2160G>A	ENSP00000412835.2:p.Lys720=
ENST00000635849.1:c.1323G>A	ENSP00000490948.1:p.Lys441=
ENST00000635957.1:c.957G>A	ENSP00000490385.1:p.Lys319=
ENST00000636930.2:c.4002G>A MANE Select	ENSP00000490491.2:p.Lys1334=
ENST00000636940.1:n.1999G>A
ENST00000637015.1:c.1370G>A
ENST00000637568.1:c.1284G>A
ENST00000637741.1:n.668G>A
ENST00000637810.1:c.1344G>A	ENSP00000489636.1:p.Lys448=
ENST00000637904.1:c.1503G>A	ENSP00000490550.1:p.Lys501=
ENST00000647938.1:c.3633G>A	ENSP00000498155.1:p.Lys1211=
ENST00000346085.9:c.3633G>A	ENSP00000344546.4:p.Lys1211=
ENST00000350026.9:c.3594G>A	ENSP00000055163.7:p.Lys1198=
ENST00000414678.6:c.2160G>A	ENSP00000412835.2:p.Lys720=
NM_017519.2:c.3594G>A	NP_059989.2:p.Lys1198=
NM_020732.3:c.3633G>A	NP_065783.3:p.Lys1211=
XM_005267069.3:c.3753G>A	XP_005267126.2:p.Lys1251=
XM_011535984.1:c.2832G>A	XP_011534286.1:p.Lys944=
XM_011535985.1:c.2652G>A	XP_011534287.1:p.Lys884=
XM_011535986.1:c.2412G>A	XP_011534288.1:p.Lys804=
XM_011535987.1:c.2031G>A	XP_011534289.1:p.Lys677=
XM_011535988.1:c.894G>A	XP_011534290.1:p.Lys298=
NM_001346813.1:c.3753G>A	NP_001333742.1:p.Lys1251=
NM_001363725.1:c.1503G>A	NP_001350654.1:p.Lys501=
XM_011535984.2:c.3963G>A	XP_011534286.2:p.Lys1321=
XM_011535988.3:c.894G>A	XP_011534290.1:p.Lys298=
XM_017011103.2:c.3864G>A	XP_016866592.1:p.Lys1288=
XM_017011104.1:c.3834G>A	XP_016866593.1:p.Lys1278=
XM_017011105.2:c.3804G>A	XP_016866594.1:p.Lys1268=
XM_017011106.2:c.3675G>A	XP_016866595.1:p.Lys1225=
XM_017011107.2:c.3654G>A	XP_016866596.1:p.Lys1218=
XR_002956289.1:n.4046G>A
NM_001363725.2:c.1503G>A	NP_001350654.1:p.Lys501=
NM_001371656.1:c.3882G>A	NP_001358585.1:p.Lys1294=
NM_001374820.1:c.3882G>A	NP_001361749.1:p.Lys1294=
NM_001374828.1:c.4002G>A MANE Select	NP_001361757.1:p.Lys1334=
NM_017519.3:c.3843G>A	NP_059989.3:p.Lys1281=