Canonical Allele Identifier: CA366239627

Gene: ARID1B

Linked Data

• dbSNP Id: rs1163916797
• MyVariant Identifiers: chr6:g.157519973G>T (hg19) ; chr6:g.157198839G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198839G>T , CM000668.2:g.157198839G>T	GRCh38
NC_000006.11:g.157519973G>T , CM000668.1:g.157519973G>T	GRCh37
NC_000006.10:g.157561665G>T	NCBI36
NG_032093.1:g.425910G>T
NG_032093.2:g.425910G>T
NG_066624.1:g.427814G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4252G>T	ENSP00000055163.8:p.Gly1418Cys
ENST00000414678.8:c.4321G>T	ENSP00000412835.3:p.Gly1441Cys
ENST00000637015.2:c.4540G>T	ENSP00000489729.2:p.Gly1514Cys
ENST00000346085.10:c.4291G>T	ENSP00000344546.5:p.Gly1431Cys
ENST00000350026.10:c.4003G>T	ENSP00000055163.7:p.Gly1335Cys
ENST00000414678.7:c.2569G>T	ENSP00000412835.2:p.Gly857Cys
ENST00000635849.1:c.1732G>T	ENSP00000490948.1:p.Gly578Cys
ENST00000635957.1:c.1363G>T	ENSP00000490385.1:p.Gly455Cys
ENST00000636227.1:n.2874G>T
ENST00000636254.1:n.331G>T
ENST00000636930.2:c.4411G>T MANE Select	ENSP00000490491.2:p.Gly1471Cys
ENST00000636940.1:n.2408G>T
ENST00000637015.1:c.1779G>T
ENST00000637568.1:c.1693G>T
ENST00000637741.1:n.1077G>T
ENST00000637810.1:c.1753G>T	ENSP00000489636.1:p.Gly585Cys
ENST00000637904.1:c.1912G>T	ENSP00000490550.1:p.Gly638Cys
ENST00000647938.1:c.4042G>T	ENSP00000498155.1:p.Gly1348Cys
ENST00000346085.9:c.4042G>T	ENSP00000344546.4:p.Gly1348Cys
ENST00000350026.9:c.4003G>T	ENSP00000055163.7:p.Gly1335Cys
ENST00000414678.6:c.2569G>T	ENSP00000412835.2:p.Gly857Cys
NM_017519.2:c.4003G>T	NP_059989.2:p.Gly1335Cys
NM_020732.3:c.4042G>T	NP_065783.3:p.Gly1348Cys
XM_005267069.3:c.4162G>T	XP_005267126.2:p.Gly1388Cys
XM_011535984.1:c.3241G>T	XP_011534286.1:p.Gly1081Cys
XM_011535985.1:c.3061G>T	XP_011534287.1:p.Gly1021Cys
XM_011535986.1:c.2821G>T	XP_011534288.1:p.Gly941Cys
XM_011535987.1:c.2440G>T	XP_011534289.1:p.Gly814Cys
XM_011535988.1:c.1303G>T	XP_011534290.1:p.Gly435Cys
NM_001346813.1:c.4162G>T	NP_001333742.1:p.Gly1388Cys
NM_001363725.1:c.1912G>T	NP_001350654.1:p.Gly638Cys
XM_011535984.2:c.4372G>T	XP_011534286.2:p.Gly1458Cys
XM_011535988.3:c.1303G>T	XP_011534290.1:p.Gly435Cys
XM_017011103.2:c.4273G>T	XP_016866592.1:p.Gly1425Cys
XM_017011104.1:c.4243G>T	XP_016866593.1:p.Gly1415Cys
XM_017011105.2:c.4213G>T	XP_016866594.1:p.Gly1405Cys
XM_017011106.2:c.4084G>T	XP_016866595.1:p.Gly1362Cys
XM_017011107.2:c.4063G>T	XP_016866596.1:p.Gly1355Cys
XR_002956289.1:n.4427-1866G>T
NM_001363725.2:c.1912G>T	NP_001350654.1:p.Gly638Cys
NM_001371656.1:c.4291G>T	NP_001358585.1:p.Gly1431Cys
NM_001374820.1:c.4291G>T	NP_001361749.1:p.Gly1431Cys
NM_001374828.1:c.4411G>T MANE Select	NP_001361757.1:p.Gly1471Cys
NM_017519.3:c.4252G>T	NP_059989.3:p.Gly1418Cys