Canonical Allele Identifier: CA366241378

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522121T>A (hg19) ; chr6:g.157200987T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200987T>A , CM000668.2:g.157200987T>A	GRCh38
NC_000006.11:g.157522121T>A , CM000668.1:g.157522121T>A	GRCh37
NC_000006.10:g.157563813T>A	NCBI36
NG_032093.1:g.428058T>A
NG_032093.2:g.428058T>A
NG_066624.1:g.429962T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4603T>A	ENSP00000055163.8:p.Trp1535Arg
ENST00000414678.8:c.4672T>A	ENSP00000412835.3:p.Trp1558Arg
ENST00000637015.2:c.4891T>A	ENSP00000489729.2:p.Trp1631Arg
ENST00000346085.10:c.4642T>A	ENSP00000344546.5:p.Trp1548Arg
ENST00000350026.10:c.4354T>A	ENSP00000055163.7:p.Trp1452Arg
ENST00000414678.7:c.2920T>A	ENSP00000412835.2:p.Trp974Arg
ENST00000635849.1:c.2083T>A	ENSP00000490948.1:p.Trp695Arg
ENST00000635957.1:c.1714T>A	ENSP00000490385.1:p.Trp572Arg
ENST00000636227.1:n.3225T>A
ENST00000636254.1:n.682T>A
ENST00000636930.2:c.4762T>A MANE Select	ENSP00000490491.2:p.Trp1588Arg
ENST00000636940.1:n.2759T>A
ENST00000637015.1:c.2130T>A
ENST00000637568.1:c.2044T>A
ENST00000637741.1:n.1428T>A
ENST00000637810.1:c.2104T>A	ENSP00000489636.1:p.Trp702Arg
ENST00000637904.1:c.2263T>A	ENSP00000490550.1:p.Trp755Arg
ENST00000647938.1:c.4393T>A	ENSP00000498155.1:p.Trp1465Arg
ENST00000346085.9:c.4393T>A	ENSP00000344546.4:p.Trp1465Arg
ENST00000350026.9:c.4354T>A	ENSP00000055163.7:p.Trp1452Arg
ENST00000414678.6:c.2920T>A	ENSP00000412835.2:p.Trp974Arg
NM_017519.2:c.4354T>A	NP_059989.2:p.Trp1452Arg
NM_020732.3:c.4393T>A	NP_065783.3:p.Trp1465Arg
XM_005267069.3:c.4513T>A	XP_005267126.2:p.Trp1505Arg
XM_011535984.1:c.3592T>A	XP_011534286.1:p.Trp1198Arg
XM_011535985.1:c.3412T>A	XP_011534287.1:p.Trp1138Arg
XM_011535986.1:c.3172T>A	XP_011534288.1:p.Trp1058Arg
XM_011535987.1:c.2791T>A	XP_011534289.1:p.Trp931Arg
XM_011535988.1:c.1654T>A	XP_011534290.1:p.Trp552Arg
NM_001346813.1:c.4513T>A	NP_001333742.1:p.Trp1505Arg
NM_001363725.1:c.2263T>A	NP_001350654.1:p.Trp755Arg
XM_011535984.2:c.4723T>A	XP_011534286.2:p.Trp1575Arg
XM_011535988.3:c.1654T>A	XP_011534290.1:p.Trp552Arg
XM_017011103.2:c.4624T>A	XP_016866592.1:p.Trp1542Arg
XM_017011104.1:c.4594T>A	XP_016866593.1:p.Trp1532Arg
XM_017011105.2:c.4564T>A	XP_016866594.1:p.Trp1522Arg
XM_017011106.2:c.4435T>A	XP_016866595.1:p.Trp1479Arg
XM_017011107.2:c.4414T>A	XP_016866596.1:p.Trp1472Arg
XR_002956289.1:n.4709T>A
NM_001363725.2:c.2263T>A	NP_001350654.1:p.Trp755Arg
NM_001371656.1:c.4642T>A	NP_001358585.1:p.Trp1548Arg
NM_001374820.1:c.4642T>A	NP_001361749.1:p.Trp1548Arg
NM_001374828.1:c.4762T>A MANE Select	NP_001361757.1:p.Trp1588Arg
NM_017519.3:c.4603T>A	NP_059989.3:p.Trp1535Arg