Canonical Allele Identifier: CA452978093

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522270T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201136T>A , CM000668.2:g.157201136T>A	GRCh38
NC_000006.11:g.157522270T>A , CM000668.1:g.157522270T>A	GRCh37
NC_000006.10:g.157563962T>A	NCBI36
NG_032093.1:g.428207T>A
NG_032093.2:g.428207T>A
NG_066624.1:g.430111T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4752T>A	ENSP00000055163.8:p.Ser1584=
ENST00000414678.8:c.4821T>A	ENSP00000412835.3:p.Ser1607=
ENST00000637015.2:c.5040T>A	ENSP00000489729.2:p.Ser1680=
ENST00000346085.10:c.4791T>A	ENSP00000344546.5:p.Ser1597=
ENST00000350026.10:c.4503T>A	ENSP00000055163.7:p.Ser1501=
ENST00000414678.7:c.3069T>A	ENSP00000412835.2:p.Ser1023=
ENST00000635849.1:c.2232T>A	ENSP00000490948.1:p.Ser744=
ENST00000635957.1:c.1863T>A	ENSP00000490385.1:p.Ser621=
ENST00000636227.1:n.3374T>A
ENST00000636254.1:n.831T>A
ENST00000636930.2:c.4911T>A MANE Select	ENSP00000490491.2:p.Ser1637=
ENST00000636940.1:n.2908T>A
ENST00000637015.1:c.2279T>A
ENST00000637568.1:c.2193T>A
ENST00000637741.1:n.1577T>A
ENST00000637810.1:c.2253T>A	ENSP00000489636.1:p.Ser751=
ENST00000637904.1:c.2412T>A	ENSP00000490550.1:p.Ser804=
ENST00000647938.1:c.4542T>A	ENSP00000498155.1:p.Ser1514=
ENST00000346085.9:c.4542T>A	ENSP00000344546.4:p.Ser1514=
ENST00000350026.9:c.4503T>A	ENSP00000055163.7:p.Ser1501=
ENST00000414678.6:c.3069T>A	ENSP00000412835.2:p.Ser1023=
NM_017519.2:c.4503T>A	NP_059989.2:p.Ser1501=
NM_020732.3:c.4542T>A	NP_065783.3:p.Ser1514=
XM_005267069.3:c.4662T>A	XP_005267126.2:p.Ser1554=
XM_011535984.1:c.3741T>A	XP_011534286.1:p.Ser1247=
XM_011535985.1:c.3561T>A	XP_011534287.1:p.Ser1187=
XM_011535986.1:c.3321T>A	XP_011534288.1:p.Ser1107=
XM_011535987.1:c.2940T>A	XP_011534289.1:p.Ser980=
XM_011535988.1:c.1803T>A	XP_011534290.1:p.Ser601=
NM_001346813.1:c.4662T>A	NP_001333742.1:p.Ser1554=
NM_001363725.1:c.2412T>A	NP_001350654.1:p.Ser804=
XM_011535984.2:c.4872T>A	XP_011534286.2:p.Ser1624=
XM_011535988.3:c.1803T>A	XP_011534290.1:p.Ser601=
XM_017011103.2:c.4773T>A	XP_016866592.1:p.Ser1591=
XM_017011104.1:c.4743T>A	XP_016866593.1:p.Ser1581=
XM_017011105.2:c.4713T>A	XP_016866594.1:p.Ser1571=
XM_017011106.2:c.4584T>A	XP_016866595.1:p.Ser1528=
XM_017011107.2:c.4563T>A	XP_016866596.1:p.Ser1521=
XR_002956289.1:n.4858T>A
NM_001363725.2:c.2412T>A	NP_001350654.1:p.Ser804=
NM_001371656.1:c.4791T>A	NP_001358585.1:p.Ser1597=
NM_001374820.1:c.4791T>A	NP_001361749.1:p.Ser1597=
NM_001374828.1:c.4911T>A MANE Select	NP_001361757.1:p.Ser1637=
NM_017519.3:c.4752T>A	NP_059989.3:p.Ser1584=