Canonical Allele Identifier: CA366242282

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522361T>A (hg19) ; chr6:g.157201227T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201227T>A , CM000668.2:g.157201227T>A	GRCh38
NC_000006.11:g.157522361T>A , CM000668.1:g.157522361T>A	GRCh37
NC_000006.10:g.157564053T>A	NCBI36
NG_032093.1:g.428298T>A
NG_032093.2:g.428298T>A
NG_066624.1:g.430202T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4843T>A	ENSP00000055163.8:p.Ser1615Thr
ENST00000414678.8:c.4912T>A	ENSP00000412835.3:p.Ser1638Thr
ENST00000637015.2:c.5131T>A	ENSP00000489729.2:p.Ser1711Thr
ENST00000346085.10:c.4882T>A	ENSP00000344546.5:p.Ser1628Thr
ENST00000350026.10:c.4594T>A	ENSP00000055163.7:p.Ser1532Thr
ENST00000414678.7:c.3160T>A	ENSP00000412835.2:p.Ser1054Thr
ENST00000635849.1:c.2323T>A	ENSP00000490948.1:p.Ser775Thr
ENST00000635957.1:c.1954T>A	ENSP00000490385.1:p.Ser652Thr
ENST00000636227.1:n.3465T>A
ENST00000636254.1:n.922T>A
ENST00000636930.2:c.5002T>A MANE Select	ENSP00000490491.2:p.Ser1668Thr
ENST00000636940.1:n.2999T>A
ENST00000637015.1:c.2370T>A
ENST00000637568.1:c.2284T>A
ENST00000637741.1:n.1668T>A
ENST00000637810.1:c.2344T>A	ENSP00000489636.1:p.Ser782Thr
ENST00000637904.1:c.2503T>A	ENSP00000490550.1:p.Ser835Thr
ENST00000647938.1:c.4633T>A	ENSP00000498155.1:p.Ser1545Thr
ENST00000346085.9:c.4633T>A	ENSP00000344546.4:p.Ser1545Thr
ENST00000350026.9:c.4594T>A	ENSP00000055163.7:p.Ser1532Thr
ENST00000414678.6:c.3160T>A	ENSP00000412835.2:p.Ser1054Thr
NM_017519.2:c.4594T>A	NP_059989.2:p.Ser1532Thr
NM_020732.3:c.4633T>A	NP_065783.3:p.Ser1545Thr
XM_005267069.3:c.4753T>A	XP_005267126.2:p.Ser1585Thr
XM_011535984.1:c.3832T>A	XP_011534286.1:p.Ser1278Thr
XM_011535985.1:c.3652T>A	XP_011534287.1:p.Ser1218Thr
XM_011535986.1:c.3412T>A	XP_011534288.1:p.Ser1138Thr
XM_011535987.1:c.3031T>A	XP_011534289.1:p.Ser1011Thr
XM_011535988.1:c.1894T>A	XP_011534290.1:p.Ser632Thr
NM_001346813.1:c.4753T>A	NP_001333742.1:p.Ser1585Thr
NM_001363725.1:c.2503T>A	NP_001350654.1:p.Ser835Thr
XM_011535984.2:c.4963T>A	XP_011534286.2:p.Ser1655Thr
XM_011535988.3:c.1894T>A	XP_011534290.1:p.Ser632Thr
XM_017011103.2:c.4864T>A	XP_016866592.1:p.Ser1622Thr
XM_017011104.1:c.4834T>A	XP_016866593.1:p.Ser1612Thr
XM_017011105.2:c.4804T>A	XP_016866594.1:p.Ser1602Thr
XM_017011106.2:c.4675T>A	XP_016866595.1:p.Ser1559Thr
XM_017011107.2:c.4654T>A	XP_016866596.1:p.Ser1552Thr
XR_002956289.1:n.4949T>A
NM_001363725.2:c.2503T>A	NP_001350654.1:p.Ser835Thr
NM_001371656.1:c.4882T>A	NP_001358585.1:p.Ser1628Thr
NM_001374820.1:c.4882T>A	NP_001361749.1:p.Ser1628Thr
NM_001374828.1:c.5002T>A MANE Select	NP_001361757.1:p.Ser1668Thr
NM_017519.3:c.4843T>A	NP_059989.3:p.Ser1615Thr