Canonical Allele Identifier: CA452781587

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511181A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190047A>T , CM000668.2:g.157190047A>T	GRCh38
NC_000006.11:g.157511181A>T , CM000668.1:g.157511181A>T	GRCh37
NC_000006.10:g.157552873A>T	NCBI36
NG_032093.1:g.417118A>T
NG_032093.2:g.417118A>T
NG_066624.1:g.419022A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3909A>T	ENSP00000055163.8:p.Thr1303=
ENST00000414678.8:c.3978A>T	ENSP00000412835.3:p.Thr1326=
ENST00000637015.2:c.4197A>T	ENSP00000489729.2:p.Thr1399=
ENST00000346085.10:c.3948A>T	ENSP00000344546.5:p.Thr1316=
ENST00000350026.10:c.3660A>T	ENSP00000055163.7:p.Thr1220=
ENST00000414678.7:c.2226A>T	ENSP00000412835.2:p.Thr742=
ENST00000635849.1:c.1389A>T	ENSP00000490948.1:p.Thr463=
ENST00000635957.1:c.1020A>T	ENSP00000490385.1:p.Thr340=
ENST00000636930.2:c.4068A>T MANE Select	ENSP00000490491.2:p.Thr1356=
ENST00000636940.1:n.2065A>T
ENST00000637015.1:c.1436A>T
ENST00000637568.1:c.1350A>T
ENST00000637741.1:n.734A>T
ENST00000637810.1:c.1410A>T	ENSP00000489636.1:p.Thr470=
ENST00000637904.1:c.1569A>T	ENSP00000490550.1:p.Thr523=
ENST00000647938.1:c.3699A>T	ENSP00000498155.1:p.Thr1233=
ENST00000346085.9:c.3699A>T	ENSP00000344546.4:p.Thr1233=
ENST00000350026.9:c.3660A>T	ENSP00000055163.7:p.Thr1220=
ENST00000414678.6:c.2226A>T	ENSP00000412835.2:p.Thr742=
NM_017519.2:c.3660A>T	NP_059989.2:p.Thr1220=
NM_020732.3:c.3699A>T	NP_065783.3:p.Thr1233=
XM_005267069.3:c.3819A>T	XP_005267126.2:p.Thr1273=
XM_011535984.1:c.2898A>T	XP_011534286.1:p.Thr966=
XM_011535985.1:c.2718A>T	XP_011534287.1:p.Thr906=
XM_011535986.1:c.2478A>T	XP_011534288.1:p.Thr826=
XM_011535987.1:c.2097A>T	XP_011534289.1:p.Thr699=
XM_011535988.1:c.960A>T	XP_011534290.1:p.Thr320=
NM_001346813.1:c.3819A>T	NP_001333742.1:p.Thr1273=
NM_001363725.1:c.1569A>T	NP_001350654.1:p.Thr523=
XM_011535984.2:c.4029A>T	XP_011534286.2:p.Thr1343=
XM_011535988.3:c.960A>T	XP_011534290.1:p.Thr320=
XM_017011103.2:c.3930A>T	XP_016866592.1:p.Thr1310=
XM_017011104.1:c.3900A>T	XP_016866593.1:p.Thr1300=
XM_017011105.2:c.3870A>T	XP_016866594.1:p.Thr1290=
XM_017011106.2:c.3741A>T	XP_016866595.1:p.Thr1247=
XM_017011107.2:c.3720A>T	XP_016866596.1:p.Thr1240=
XR_002956289.1:n.4112A>T
NM_001363725.2:c.1569A>T	NP_001350654.1:p.Thr523=
NM_001371656.1:c.3948A>T	NP_001358585.1:p.Thr1316=
NM_001374820.1:c.3948A>T	NP_001361749.1:p.Thr1316=
NM_001374828.1:c.4068A>T MANE Select	NP_001361757.1:p.Thr1356=
NM_017519.3:c.3909A>T	NP_059989.3:p.Thr1303=