Canonical Allele Identifier: CA452783946

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366301
• MyVariant Identifiers: chr6:g.157519993A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198859A>T , CM000668.2:g.157198859A>T	GRCh38
NC_000006.11:g.157519993A>T , CM000668.1:g.157519993A>T	GRCh37
NC_000006.10:g.157561685A>T	NCBI36
NG_032093.1:g.425930A>T
NG_032093.2:g.425930A>T
NG_066624.1:g.427834A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4272A>T	ENSP00000055163.8:p.Gly1424=
ENST00000414678.8:c.4341A>T	ENSP00000412835.3:p.Gly1447=
ENST00000637015.2:c.4560A>T	ENSP00000489729.2:p.Gly1520=
ENST00000346085.10:c.4311A>T	ENSP00000344546.5:p.Gly1437=
ENST00000350026.10:c.4023A>T	ENSP00000055163.7:p.Gly1341=
ENST00000414678.7:c.2589A>T	ENSP00000412835.2:p.Gly863=
ENST00000635849.1:c.1752A>T	ENSP00000490948.1:p.Gly584=
ENST00000635957.1:c.1383A>T	ENSP00000490385.1:p.Gly461=
ENST00000636227.1:n.2894A>T
ENST00000636254.1:n.351A>T
ENST00000636930.2:c.4431A>T MANE Select	ENSP00000490491.2:p.Gly1477=
ENST00000636940.1:n.2428A>T
ENST00000637015.1:c.1799A>T
ENST00000637568.1:c.1713A>T
ENST00000637741.1:n.1097A>T
ENST00000637810.1:c.1773A>T	ENSP00000489636.1:p.Gly591=
ENST00000637904.1:c.1932A>T	ENSP00000490550.1:p.Gly644=
ENST00000647938.1:c.4062A>T	ENSP00000498155.1:p.Gly1354=
ENST00000346085.9:c.4062A>T	ENSP00000344546.4:p.Gly1354=
ENST00000350026.9:c.4023A>T	ENSP00000055163.7:p.Gly1341=
ENST00000414678.6:c.2589A>T	ENSP00000412835.2:p.Gly863=
NM_017519.2:c.4023A>T	NP_059989.2:p.Gly1341=
NM_020732.3:c.4062A>T	NP_065783.3:p.Gly1354=
XM_005267069.3:c.4182A>T	XP_005267126.2:p.Gly1394=
XM_011535984.1:c.3261A>T	XP_011534286.1:p.Gly1087=
XM_011535985.1:c.3081A>T	XP_011534287.1:p.Gly1027=
XM_011535986.1:c.2841A>T	XP_011534288.1:p.Gly947=
XM_011535987.1:c.2460A>T	XP_011534289.1:p.Gly820=
XM_011535988.1:c.1323A>T	XP_011534290.1:p.Gly441=
NM_001346813.1:c.4182A>T	NP_001333742.1:p.Gly1394=
NM_001363725.1:c.1932A>T	NP_001350654.1:p.Gly644=
XM_011535984.2:c.4392A>T	XP_011534286.2:p.Gly1464=
XM_011535988.3:c.1323A>T	XP_011534290.1:p.Gly441=
XM_017011103.2:c.4293A>T	XP_016866592.1:p.Gly1431=
XM_017011104.1:c.4263A>T	XP_016866593.1:p.Gly1421=
XM_017011105.2:c.4233A>T	XP_016866594.1:p.Gly1411=
XM_017011106.2:c.4104A>T	XP_016866595.1:p.Gly1368=
XM_017011107.2:c.4083A>T	XP_016866596.1:p.Gly1361=
XR_002956289.1:n.4427-1846A>T
NM_001363725.2:c.1932A>T	NP_001350654.1:p.Gly644=
NM_001371656.1:c.4311A>T	NP_001358585.1:p.Gly1437=
NM_001374820.1:c.4311A>T	NP_001361749.1:p.Gly1437=
NM_001374828.1:c.4431A>T MANE Select	NP_001361757.1:p.Gly1477=
NM_017519.3:c.4272A>T	NP_059989.3:p.Gly1424=