Canonical Allele Identifier: CA366234014

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510787T>A (hg19) ; chr6:g.157189653T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189653T>A , CM000668.2:g.157189653T>A	GRCh38
NC_000006.11:g.157510787T>A , CM000668.1:g.157510787T>A	GRCh37
NC_000006.10:g.157552479T>A	NCBI36
NG_032093.1:g.416724T>A
NG_032093.2:g.416724T>A
NG_066624.1:g.418628T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3772T>A	ENSP00000055163.8:p.Ser1258Thr
ENST00000414678.8:c.3841T>A	ENSP00000412835.3:p.Ser1281Thr
ENST00000637015.2:c.4060T>A	ENSP00000489729.2:p.Ser1354Thr
ENST00000346085.10:c.3811T>A	ENSP00000344546.5:p.Ser1271Thr
ENST00000350026.10:c.3523T>A	ENSP00000055163.7:p.Ser1175Thr
ENST00000414678.7:c.2089T>A	ENSP00000412835.2:p.Ser697Thr
ENST00000635849.1:c.1252T>A	ENSP00000490948.1:p.Ser418Thr
ENST00000635957.1:c.886T>A	ENSP00000490385.1:p.Ser296Thr
ENST00000636930.2:c.3931T>A MANE Select	ENSP00000490491.2:p.Ser1311Thr
ENST00000636940.1:n.1928T>A
ENST00000637015.1:c.1299T>A
ENST00000637568.1:c.1213T>A
ENST00000637741.1:n.597T>A
ENST00000637810.1:c.1273T>A	ENSP00000489636.1:p.Ser425Thr
ENST00000637904.1:c.1432T>A	ENSP00000490550.1:p.Ser478Thr
ENST00000647938.1:c.3562T>A	ENSP00000498155.1:p.Ser1188Thr
ENST00000346085.9:c.3562T>A	ENSP00000344546.4:p.Ser1188Thr
ENST00000350026.9:c.3523T>A	ENSP00000055163.7:p.Ser1175Thr
ENST00000414678.6:c.2089T>A	ENSP00000412835.2:p.Ser697Thr
NM_017519.2:c.3523T>A	NP_059989.2:p.Ser1175Thr
NM_020732.3:c.3562T>A	NP_065783.3:p.Ser1188Thr
XM_005267069.3:c.3682T>A	XP_005267126.2:p.Ser1228Thr
XM_011535984.1:c.2761T>A	XP_011534286.1:p.Ser921Thr
XM_011535985.1:c.2581T>A	XP_011534287.1:p.Ser861Thr
XM_011535986.1:c.2341T>A	XP_011534288.1:p.Ser781Thr
XM_011535987.1:c.1960T>A	XP_011534289.1:p.Ser654Thr
XM_011535988.1:c.823T>A	XP_011534290.1:p.Ser275Thr
NM_001346813.1:c.3682T>A	NP_001333742.1:p.Ser1228Thr
NM_001363725.1:c.1432T>A	NP_001350654.1:p.Ser478Thr
XM_011535984.2:c.3892T>A	XP_011534286.2:p.Ser1298Thr
XM_011535988.3:c.823T>A	XP_011534290.1:p.Ser275Thr
XM_017011103.2:c.3793T>A	XP_016866592.1:p.Ser1265Thr
XM_017011104.1:c.3763T>A	XP_016866593.1:p.Ser1255Thr
XM_017011105.2:c.3733T>A	XP_016866594.1:p.Ser1245Thr
XM_017011106.2:c.3604T>A	XP_016866595.1:p.Ser1202Thr
XM_017011107.2:c.3583T>A	XP_016866596.1:p.Ser1195Thr
XR_002956289.1:n.3975T>A
NM_001363725.2:c.1432T>A	NP_001350654.1:p.Ser478Thr
NM_001371656.1:c.3811T>A	NP_001358585.1:p.Ser1271Thr
NM_001374820.1:c.3811T>A	NP_001361749.1:p.Ser1271Thr
NM_001374828.1:c.3931T>A MANE Select	NP_001361757.1:p.Ser1311Thr
NM_017519.3:c.3772T>A	NP_059989.3:p.Ser1258Thr