Canonical Allele Identifier: CA366234120

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510835G>T (hg19) ; chr6:g.157189701G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189701G>T , CM000668.2:g.157189701G>T	GRCh38
NC_000006.11:g.157510835G>T , CM000668.1:g.157510835G>T	GRCh37
NC_000006.10:g.157552527G>T	NCBI36
NG_032093.1:g.416772G>T
NG_032093.2:g.416772G>T
NG_066624.1:g.418676G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3820G>T	ENSP00000055163.8:p.Ala1274Ser
ENST00000414678.8:c.3889G>T	ENSP00000412835.3:p.Ala1297Ser
ENST00000637015.2:c.4108G>T	ENSP00000489729.2:p.Ala1370Ser
ENST00000346085.10:c.3859G>T	ENSP00000344546.5:p.Ala1287Ser
ENST00000350026.10:c.3571G>T	ENSP00000055163.7:p.Ala1191Ser
ENST00000414678.7:c.2137G>T	ENSP00000412835.2:p.Ala713Ser
ENST00000635849.1:c.1300G>T	ENSP00000490948.1:p.Ala434Ser
ENST00000635957.1:c.934G>T	ENSP00000490385.1:p.Ala312Ser
ENST00000636930.2:c.3979G>T MANE Select	ENSP00000490491.2:p.Ala1327Ser
ENST00000636940.1:n.1976G>T
ENST00000637015.1:c.1347G>T
ENST00000637568.1:c.1261G>T
ENST00000637741.1:n.645G>T
ENST00000637810.1:c.1321G>T	ENSP00000489636.1:p.Ala441Ser
ENST00000637904.1:c.1480G>T	ENSP00000490550.1:p.Ala494Ser
ENST00000647938.1:c.3610G>T	ENSP00000498155.1:p.Ala1204Ser
ENST00000346085.9:c.3610G>T	ENSP00000344546.4:p.Ala1204Ser
ENST00000350026.9:c.3571G>T	ENSP00000055163.7:p.Ala1191Ser
ENST00000414678.6:c.2137G>T	ENSP00000412835.2:p.Ala713Ser
NM_017519.2:c.3571G>T	NP_059989.2:p.Ala1191Ser
NM_020732.3:c.3610G>T	NP_065783.3:p.Ala1204Ser
XM_005267069.3:c.3730G>T	XP_005267126.2:p.Ala1244Ser
XM_011535984.1:c.2809G>T	XP_011534286.1:p.Ala937Ser
XM_011535985.1:c.2629G>T	XP_011534287.1:p.Ala877Ser
XM_011535986.1:c.2389G>T	XP_011534288.1:p.Ala797Ser
XM_011535987.1:c.2008G>T	XP_011534289.1:p.Ala670Ser
XM_011535988.1:c.871G>T	XP_011534290.1:p.Ala291Ser
NM_001346813.1:c.3730G>T	NP_001333742.1:p.Ala1244Ser
NM_001363725.1:c.1480G>T	NP_001350654.1:p.Ala494Ser
XM_011535984.2:c.3940G>T	XP_011534286.2:p.Ala1314Ser
XM_011535988.3:c.871G>T	XP_011534290.1:p.Ala291Ser
XM_017011103.2:c.3841G>T	XP_016866592.1:p.Ala1281Ser
XM_017011104.1:c.3811G>T	XP_016866593.1:p.Ala1271Ser
XM_017011105.2:c.3781G>T	XP_016866594.1:p.Ala1261Ser
XM_017011106.2:c.3652G>T	XP_016866595.1:p.Ala1218Ser
XM_017011107.2:c.3631G>T	XP_016866596.1:p.Ala1211Ser
XR_002956289.1:n.4023G>T
NM_001363725.2:c.1480G>T	NP_001350654.1:p.Ala494Ser
NM_001371656.1:c.3859G>T	NP_001358585.1:p.Ala1287Ser
NM_001374820.1:c.3859G>T	NP_001361749.1:p.Ala1287Ser
NM_001374828.1:c.3979G>T MANE Select	NP_001361757.1:p.Ala1327Ser
NM_017519.3:c.3820G>T	NP_059989.3:p.Ala1274Ser