Canonical Allele Identifier: CA366234894

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511200T>A (hg19) ; chr6:g.157190066T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190066T>A , CM000668.2:g.157190066T>A	GRCh38
NC_000006.11:g.157511200T>A , CM000668.1:g.157511200T>A	GRCh37
NC_000006.10:g.157552892T>A	NCBI36
NG_032093.1:g.417137T>A
NG_032093.2:g.417137T>A
NG_066624.1:g.419041T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3928T>A	ENSP00000055163.8:p.Phe1310Ile
ENST00000414678.8:c.3997T>A	ENSP00000412835.3:p.Phe1333Ile
ENST00000637015.2:c.4216T>A	ENSP00000489729.2:p.Phe1406Ile
ENST00000346085.10:c.3967T>A	ENSP00000344546.5:p.Phe1323Ile
ENST00000350026.10:c.3679T>A	ENSP00000055163.7:p.Phe1227Ile
ENST00000414678.7:c.2245T>A	ENSP00000412835.2:p.Phe749Ile
ENST00000635849.1:c.1408T>A	ENSP00000490948.1:p.Phe470Ile
ENST00000635957.1:c.1039T>A	ENSP00000490385.1:p.Phe347Ile
ENST00000636930.2:c.4087T>A MANE Select	ENSP00000490491.2:p.Phe1363Ile
ENST00000636940.1:n.2084T>A
ENST00000637015.1:c.1455T>A
ENST00000637568.1:c.1369T>A
ENST00000637741.1:n.753T>A
ENST00000637810.1:c.1429T>A	ENSP00000489636.1:p.Phe477Ile
ENST00000637904.1:c.1588T>A	ENSP00000490550.1:p.Phe530Ile
ENST00000647938.1:c.3718T>A	ENSP00000498155.1:p.Phe1240Ile
ENST00000346085.9:c.3718T>A	ENSP00000344546.4:p.Phe1240Ile
ENST00000350026.9:c.3679T>A	ENSP00000055163.7:p.Phe1227Ile
ENST00000414678.6:c.2245T>A	ENSP00000412835.2:p.Phe749Ile
NM_017519.2:c.3679T>A	NP_059989.2:p.Phe1227Ile
NM_020732.3:c.3718T>A	NP_065783.3:p.Phe1240Ile
XM_005267069.3:c.3838T>A	XP_005267126.2:p.Phe1280Ile
XM_011535984.1:c.2917T>A	XP_011534286.1:p.Phe973Ile
XM_011535985.1:c.2737T>A	XP_011534287.1:p.Phe913Ile
XM_011535986.1:c.2497T>A	XP_011534288.1:p.Phe833Ile
XM_011535987.1:c.2116T>A	XP_011534289.1:p.Phe706Ile
XM_011535988.1:c.979T>A	XP_011534290.1:p.Phe327Ile
NM_001346813.1:c.3838T>A	NP_001333742.1:p.Phe1280Ile
NM_001363725.1:c.1588T>A	NP_001350654.1:p.Phe530Ile
XM_011535984.2:c.4048T>A	XP_011534286.2:p.Phe1350Ile
XM_011535988.3:c.979T>A	XP_011534290.1:p.Phe327Ile
XM_017011103.2:c.3949T>A	XP_016866592.1:p.Phe1317Ile
XM_017011104.1:c.3919T>A	XP_016866593.1:p.Phe1307Ile
XM_017011105.2:c.3889T>A	XP_016866594.1:p.Phe1297Ile
XM_017011106.2:c.3760T>A	XP_016866595.1:p.Phe1254Ile
XM_017011107.2:c.3739T>A	XP_016866596.1:p.Phe1247Ile
XR_002956289.1:n.4131T>A
NM_001363725.2:c.1588T>A	NP_001350654.1:p.Phe530Ile
NM_001371656.1:c.3967T>A	NP_001358585.1:p.Phe1323Ile
NM_001374820.1:c.3967T>A	NP_001361749.1:p.Phe1323Ile
NM_001374828.1:c.4087T>A MANE Select	NP_001361757.1:p.Phe1363Ile
NM_017519.3:c.3928T>A	NP_059989.3:p.Phe1310Ile