Canonical Allele Identifier: CA366242050

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522257G>T (hg19) ; chr6:g.157201123G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201123G>T , CM000668.2:g.157201123G>T	GRCh38
NC_000006.11:g.157522257G>T , CM000668.1:g.157522257G>T	GRCh37
NC_000006.10:g.157563949G>T	NCBI36
NG_032093.1:g.428194G>T
NG_032093.2:g.428194G>T
NG_066624.1:g.430098G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4739G>T	ENSP00000055163.8:p.Ser1580Ile
ENST00000414678.8:c.4808G>T	ENSP00000412835.3:p.Ser1603Ile
ENST00000637015.2:c.5027G>T	ENSP00000489729.2:p.Ser1676Ile
ENST00000346085.10:c.4778G>T	ENSP00000344546.5:p.Ser1593Ile
ENST00000350026.10:c.4490G>T	ENSP00000055163.7:p.Ser1497Ile
ENST00000414678.7:c.3056G>T	ENSP00000412835.2:p.Ser1019Ile
ENST00000635849.1:c.2219G>T	ENSP00000490948.1:p.Ser740Ile
ENST00000635957.1:c.1850G>T	ENSP00000490385.1:p.Ser617Ile
ENST00000636227.1:n.3361G>T
ENST00000636254.1:n.818G>T
ENST00000636930.2:c.4898G>T MANE Select	ENSP00000490491.2:p.Ser1633Ile
ENST00000636940.1:n.2895G>T
ENST00000637015.1:c.2266G>T
ENST00000637568.1:c.2180G>T
ENST00000637741.1:n.1564G>T
ENST00000637810.1:c.2240G>T	ENSP00000489636.1:p.Ser747Ile
ENST00000637904.1:c.2399G>T	ENSP00000490550.1:p.Ser800Ile
ENST00000647938.1:c.4529G>T	ENSP00000498155.1:p.Ser1510Ile
ENST00000346085.9:c.4529G>T	ENSP00000344546.4:p.Ser1510Ile
ENST00000350026.9:c.4490G>T	ENSP00000055163.7:p.Ser1497Ile
ENST00000414678.6:c.3056G>T	ENSP00000412835.2:p.Ser1019Ile
NM_017519.2:c.4490G>T	NP_059989.2:p.Ser1497Ile
NM_020732.3:c.4529G>T	NP_065783.3:p.Ser1510Ile
XM_005267069.3:c.4649G>T	XP_005267126.2:p.Ser1550Ile
XM_011535984.1:c.3728G>T	XP_011534286.1:p.Ser1243Ile
XM_011535985.1:c.3548G>T	XP_011534287.1:p.Ser1183Ile
XM_011535986.1:c.3308G>T	XP_011534288.1:p.Ser1103Ile
XM_011535987.1:c.2927G>T	XP_011534289.1:p.Ser976Ile
XM_011535988.1:c.1790G>T	XP_011534290.1:p.Ser597Ile
NM_001346813.1:c.4649G>T	NP_001333742.1:p.Ser1550Ile
NM_001363725.1:c.2399G>T	NP_001350654.1:p.Ser800Ile
XM_011535984.2:c.4859G>T	XP_011534286.2:p.Ser1620Ile
XM_011535988.3:c.1790G>T	XP_011534290.1:p.Ser597Ile
XM_017011103.2:c.4760G>T	XP_016866592.1:p.Ser1587Ile
XM_017011104.1:c.4730G>T	XP_016866593.1:p.Ser1577Ile
XM_017011105.2:c.4700G>T	XP_016866594.1:p.Ser1567Ile
XM_017011106.2:c.4571G>T	XP_016866595.1:p.Ser1524Ile
XM_017011107.2:c.4550G>T	XP_016866596.1:p.Ser1517Ile
XR_002956289.1:n.4845G>T
NM_001363725.2:c.2399G>T	NP_001350654.1:p.Ser800Ile
NM_001371656.1:c.4778G>T	NP_001358585.1:p.Ser1593Ile
NM_001374820.1:c.4778G>T	NP_001361749.1:p.Ser1593Ile
NM_001374828.1:c.4898G>T MANE Select	NP_001361757.1:p.Ser1633Ile
NM_017519.3:c.4739G>T	NP_059989.3:p.Ser1580Ile