Canonical Allele Identifier: CA366241753

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522193C>A (hg19) ; chr6:g.157201059C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201059C>A , CM000668.2:g.157201059C>A	GRCh38
NC_000006.11:g.157522193C>A , CM000668.1:g.157522193C>A	GRCh37
NC_000006.10:g.157563885C>A	NCBI36
NG_032093.1:g.428130C>A
NG_032093.2:g.428130C>A
NG_066624.1:g.430034C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4675C>A	ENSP00000055163.8:p.Pro1559Thr
ENST00000414678.8:c.4744C>A	ENSP00000412835.3:p.Pro1582Thr
ENST00000637015.2:c.4963C>A	ENSP00000489729.2:p.Pro1655Thr
ENST00000346085.10:c.4714C>A	ENSP00000344546.5:p.Pro1572Thr
ENST00000350026.10:c.4426C>A	ENSP00000055163.7:p.Pro1476Thr
ENST00000414678.7:c.2992C>A	ENSP00000412835.2:p.Pro998Thr
ENST00000635849.1:c.2155C>A	ENSP00000490948.1:p.Pro719Thr
ENST00000635957.1:c.1786C>A	ENSP00000490385.1:p.Pro596Thr
ENST00000636227.1:n.3297C>A
ENST00000636254.1:n.754C>A
ENST00000636930.2:c.4834C>A MANE Select	ENSP00000490491.2:p.Pro1612Thr
ENST00000636940.1:n.2831C>A
ENST00000637015.1:c.2202C>A
ENST00000637568.1:c.2116C>A
ENST00000637741.1:n.1500C>A
ENST00000637810.1:c.2176C>A	ENSP00000489636.1:p.Pro726Thr
ENST00000637904.1:c.2335C>A	ENSP00000490550.1:p.Pro779Thr
ENST00000647938.1:c.4465C>A	ENSP00000498155.1:p.Pro1489Thr
ENST00000346085.9:c.4465C>A	ENSP00000344546.4:p.Pro1489Thr
ENST00000350026.9:c.4426C>A	ENSP00000055163.7:p.Pro1476Thr
ENST00000414678.6:c.2992C>A	ENSP00000412835.2:p.Pro998Thr
NM_017519.2:c.4426C>A	NP_059989.2:p.Pro1476Thr
NM_020732.3:c.4465C>A	NP_065783.3:p.Pro1489Thr
XM_005267069.3:c.4585C>A	XP_005267126.2:p.Pro1529Thr
XM_011535984.1:c.3664C>A	XP_011534286.1:p.Pro1222Thr
XM_011535985.1:c.3484C>A	XP_011534287.1:p.Pro1162Thr
XM_011535986.1:c.3244C>A	XP_011534288.1:p.Pro1082Thr
XM_011535987.1:c.2863C>A	XP_011534289.1:p.Pro955Thr
XM_011535988.1:c.1726C>A	XP_011534290.1:p.Pro576Thr
NM_001346813.1:c.4585C>A	NP_001333742.1:p.Pro1529Thr
NM_001363725.1:c.2335C>A	NP_001350654.1:p.Pro779Thr
XM_011535984.2:c.4795C>A	XP_011534286.2:p.Pro1599Thr
XM_011535988.3:c.1726C>A	XP_011534290.1:p.Pro576Thr
XM_017011103.2:c.4696C>A	XP_016866592.1:p.Pro1566Thr
XM_017011104.1:c.4666C>A	XP_016866593.1:p.Pro1556Thr
XM_017011105.2:c.4636C>A	XP_016866594.1:p.Pro1546Thr
XM_017011106.2:c.4507C>A	XP_016866595.1:p.Pro1503Thr
XM_017011107.2:c.4486C>A	XP_016866596.1:p.Pro1496Thr
XR_002956289.1:n.4781C>A
NM_001363725.2:c.2335C>A	NP_001350654.1:p.Pro779Thr
NM_001371656.1:c.4714C>A	NP_001358585.1:p.Pro1572Thr
NM_001374820.1:c.4714C>A	NP_001361749.1:p.Pro1572Thr
NM_001374828.1:c.4834C>A MANE Select	NP_001361757.1:p.Pro1612Thr
NM_017519.3:c.4675C>A	NP_059989.3:p.Pro1559Thr