Canonical Allele Identifier: CA366234912

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511201T>A (hg19) ; chr6:g.157190067T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190067T>A , CM000668.2:g.157190067T>A	GRCh38
NC_000006.11:g.157511201T>A , CM000668.1:g.157511201T>A	GRCh37
NC_000006.10:g.157552893T>A	NCBI36
NG_032093.1:g.417138T>A
NG_032093.2:g.417138T>A
NG_066624.1:g.419042T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3929T>A	ENSP00000055163.8:p.Phe1310Tyr
ENST00000414678.8:c.3998T>A	ENSP00000412835.3:p.Phe1333Tyr
ENST00000637015.2:c.4217T>A	ENSP00000489729.2:p.Phe1406Tyr
ENST00000346085.10:c.3968T>A	ENSP00000344546.5:p.Phe1323Tyr
ENST00000350026.10:c.3680T>A	ENSP00000055163.7:p.Phe1227Tyr
ENST00000414678.7:c.2246T>A	ENSP00000412835.2:p.Phe749Tyr
ENST00000635849.1:c.1409T>A	ENSP00000490948.1:p.Phe470Tyr
ENST00000635957.1:c.1040T>A	ENSP00000490385.1:p.Phe347Tyr
ENST00000636930.2:c.4088T>A MANE Select	ENSP00000490491.2:p.Phe1363Tyr
ENST00000636940.1:n.2085T>A
ENST00000637015.1:c.1456T>A
ENST00000637568.1:c.1370T>A
ENST00000637741.1:n.754T>A
ENST00000637810.1:c.1430T>A	ENSP00000489636.1:p.Phe477Tyr
ENST00000637904.1:c.1589T>A	ENSP00000490550.1:p.Phe530Tyr
ENST00000647938.1:c.3719T>A	ENSP00000498155.1:p.Phe1240Tyr
ENST00000346085.9:c.3719T>A	ENSP00000344546.4:p.Phe1240Tyr
ENST00000350026.9:c.3680T>A	ENSP00000055163.7:p.Phe1227Tyr
ENST00000414678.6:c.2246T>A	ENSP00000412835.2:p.Phe749Tyr
NM_017519.2:c.3680T>A	NP_059989.2:p.Phe1227Tyr
NM_020732.3:c.3719T>A	NP_065783.3:p.Phe1240Tyr
XM_005267069.3:c.3839T>A	XP_005267126.2:p.Phe1280Tyr
XM_011535984.1:c.2918T>A	XP_011534286.1:p.Phe973Tyr
XM_011535985.1:c.2738T>A	XP_011534287.1:p.Phe913Tyr
XM_011535986.1:c.2498T>A	XP_011534288.1:p.Phe833Tyr
XM_011535987.1:c.2117T>A	XP_011534289.1:p.Phe706Tyr
XM_011535988.1:c.980T>A	XP_011534290.1:p.Phe327Tyr
NM_001346813.1:c.3839T>A	NP_001333742.1:p.Phe1280Tyr
NM_001363725.1:c.1589T>A	NP_001350654.1:p.Phe530Tyr
XM_011535984.2:c.4049T>A	XP_011534286.2:p.Phe1350Tyr
XM_011535988.3:c.980T>A	XP_011534290.1:p.Phe327Tyr
XM_017011103.2:c.3950T>A	XP_016866592.1:p.Phe1317Tyr
XM_017011104.1:c.3920T>A	XP_016866593.1:p.Phe1307Tyr
XM_017011105.2:c.3890T>A	XP_016866594.1:p.Phe1297Tyr
XM_017011106.2:c.3761T>A	XP_016866595.1:p.Phe1254Tyr
XM_017011107.2:c.3740T>A	XP_016866596.1:p.Phe1247Tyr
XR_002956289.1:n.4132T>A
NM_001363725.2:c.1589T>A	NP_001350654.1:p.Phe530Tyr
NM_001371656.1:c.3968T>A	NP_001358585.1:p.Phe1323Tyr
NM_001374820.1:c.3968T>A	NP_001361749.1:p.Phe1323Tyr
NM_001374828.1:c.4088T>A MANE Select	NP_001361757.1:p.Phe1363Tyr
NM_017519.3:c.3929T>A	NP_059989.3:p.Phe1310Tyr