Canonical Allele Identifier: CA366234414

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510910G>A (hg19) ; chr6:g.157189776G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189776G>A , CM000668.2:g.157189776G>A	GRCh38
NC_000006.11:g.157510910G>A , CM000668.1:g.157510910G>A	GRCh37
NC_000006.10:g.157552602G>A	NCBI36
NG_032093.1:g.416847G>A
NG_032093.2:g.416847G>A
NG_066624.1:g.418751G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3895G>A	ENSP00000055163.8:p.Gly1299Arg
ENST00000414678.8:c.3964G>A	ENSP00000412835.3:p.Gly1322Arg
ENST00000637015.2:c.4183G>A	ENSP00000489729.2:p.Gly1395Arg
ENST00000346085.10:c.3934G>A	ENSP00000344546.5:p.Gly1312Arg
ENST00000350026.10:c.3646G>A	ENSP00000055163.7:p.Gly1216Arg
ENST00000414678.7:c.2212G>A	ENSP00000412835.2:p.Gly738Arg
ENST00000635849.1:c.1375G>A	ENSP00000490948.1:p.Gly459Arg
ENST00000635957.1:c.1009G>A	ENSP00000490385.1:p.Gly337Arg
ENST00000636930.2:c.4054G>A MANE Select	ENSP00000490491.2:p.Gly1352Arg
ENST00000636940.1:n.2051G>A
ENST00000637015.1:c.1422G>A
ENST00000637568.1:c.1336G>A
ENST00000637741.1:n.720G>A
ENST00000637810.1:c.1396G>A	ENSP00000489636.1:p.Gly466Arg
ENST00000637904.1:c.1555G>A	ENSP00000490550.1:p.Gly519Arg
ENST00000647938.1:c.3685G>A	ENSP00000498155.1:p.Gly1229Arg
ENST00000346085.9:c.3685G>A	ENSP00000344546.4:p.Gly1229Arg
ENST00000350026.9:c.3646G>A	ENSP00000055163.7:p.Gly1216Arg
ENST00000414678.6:c.2212G>A	ENSP00000412835.2:p.Gly738Arg
NM_017519.2:c.3646G>A	NP_059989.2:p.Gly1216Arg
NM_020732.3:c.3685G>A	NP_065783.3:p.Gly1229Arg
XM_005267069.3:c.3805G>A	XP_005267126.2:p.Gly1269Arg
XM_011535984.1:c.2884G>A	XP_011534286.1:p.Gly962Arg
XM_011535985.1:c.2704G>A	XP_011534287.1:p.Gly902Arg
XM_011535986.1:c.2464G>A	XP_011534288.1:p.Gly822Arg
XM_011535987.1:c.2083G>A	XP_011534289.1:p.Gly695Arg
XM_011535988.1:c.946G>A	XP_011534290.1:p.Gly316Arg
NM_001346813.1:c.3805G>A	NP_001333742.1:p.Gly1269Arg
NM_001363725.1:c.1555G>A	NP_001350654.1:p.Gly519Arg
XM_011535984.2:c.4015G>A	XP_011534286.2:p.Gly1339Arg
XM_011535988.3:c.946G>A	XP_011534290.1:p.Gly316Arg
XM_017011103.2:c.3916G>A	XP_016866592.1:p.Gly1306Arg
XM_017011104.1:c.3886G>A	XP_016866593.1:p.Gly1296Arg
XM_017011105.2:c.3856G>A	XP_016866594.1:p.Gly1286Arg
XM_017011106.2:c.3727G>A	XP_016866595.1:p.Gly1243Arg
XM_017011107.2:c.3706G>A	XP_016866596.1:p.Gly1236Arg
XR_002956289.1:n.4098G>A
NM_001363725.2:c.1555G>A	NP_001350654.1:p.Gly519Arg
NM_001371656.1:c.3934G>A	NP_001358585.1:p.Gly1312Arg
NM_001374820.1:c.3934G>A	NP_001361749.1:p.Gly1312Arg
NM_001374828.1:c.4054G>A MANE Select	NP_001361757.1:p.Gly1352Arg
NM_017519.3:c.3895G>A	NP_059989.3:p.Gly1299Arg