Canonical Allele Identifier: CA366234419

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554232985
• MyVariant Identifiers: chr6:g.157510910G>T (hg19) ; chr6:g.157189776G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3895G>T	ENSP00000055163.8:p.Gly1299Ter
ENST00000414678.8:c.3964G>T	ENSP00000412835.3:p.Gly1322Ter
ENST00000637015.2:c.4183G>T	ENSP00000489729.2:p.Gly1395Ter
ENST00000346085.10:c.3934G>T	ENSP00000344546.5:p.Gly1312Ter
ENST00000350026.10:c.3646G>T	ENSP00000055163.7:p.Gly1216Ter
ENST00000414678.7:c.2212G>T	ENSP00000412835.2:p.Gly738Ter
ENST00000635849.1:c.1375G>T	ENSP00000490948.1:p.Gly459Ter
ENST00000635957.1:c.1009G>T	ENSP00000490385.1:p.Gly337Ter
ENST00000636930.2:c.4054G>T MANE Select	ENSP00000490491.2:p.Gly1352Ter
ENST00000636940.1:n.2051G>T
ENST00000637015.1:c.1422G>T
ENST00000637568.1:c.1336G>T
ENST00000637741.1:n.720G>T
ENST00000637810.1:c.1396G>T	ENSP00000489636.1:p.Gly466Ter
ENST00000637904.1:c.1555G>T	ENSP00000490550.1:p.Gly519Ter
ENST00000647938.1:c.3685G>T	ENSP00000498155.1:p.Gly1229Ter
ENST00000346085.9:c.3685G>T	ENSP00000344546.4:p.Gly1229Ter
ENST00000350026.9:c.3646G>T	ENSP00000055163.7:p.Gly1216Ter
ENST00000414678.6:c.2212G>T	ENSP00000412835.2:p.Gly738Ter
NM_017519.2:c.3646G>T	NP_059989.2:p.Gly1216Ter
NM_020732.3:c.3685G>T	NP_065783.3:p.Gly1229Ter
XM_005267069.3:c.3805G>T	XP_005267126.2:p.Gly1269Ter
XM_011535984.1:c.2884G>T	XP_011534286.1:p.Gly962Ter
XM_011535985.1:c.2704G>T	XP_011534287.1:p.Gly902Ter
XM_011535986.1:c.2464G>T	XP_011534288.1:p.Gly822Ter
XM_011535987.1:c.2083G>T	XP_011534289.1:p.Gly695Ter
XM_011535988.1:c.946G>T	XP_011534290.1:p.Gly316Ter
NM_001346813.1:c.3805G>T	NP_001333742.1:p.Gly1269Ter
NM_001363725.1:c.1555G>T	NP_001350654.1:p.Gly519Ter
XM_011535984.2:c.4015G>T	XP_011534286.2:p.Gly1339Ter
XM_011535988.3:c.946G>T	XP_011534290.1:p.Gly316Ter
XM_017011103.2:c.3916G>T	XP_016866592.1:p.Gly1306Ter
XM_017011104.1:c.3886G>T	XP_016866593.1:p.Gly1296Ter
XM_017011105.2:c.3856G>T	XP_016866594.1:p.Gly1286Ter
XM_017011106.2:c.3727G>T	XP_016866595.1:p.Gly1243Ter
XM_017011107.2:c.3706G>T	XP_016866596.1:p.Gly1236Ter
XR_002956289.1:n.4098G>T
NM_001363725.2:c.1555G>T	NP_001350654.1:p.Gly519Ter
NM_001371656.1:c.3934G>T	NP_001358585.1:p.Gly1312Ter
NM_001374820.1:c.3934G>T	NP_001361749.1:p.Gly1312Ter
NM_001374828.1:c.4054G>T MANE Select	NP_001361757.1:p.Gly1352Ter
NM_017519.3:c.3895G>T	NP_059989.3:p.Gly1299Ter