Canonical Allele Identifier: CA452978343

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522459T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201325T>G , CM000668.2:g.157201325T>G	GRCh38
NC_000006.11:g.157522459T>G , CM000668.1:g.157522459T>G	GRCh37
NC_000006.10:g.157564151T>G	NCBI36
NG_032093.1:g.428396T>G
NG_032093.2:g.428396T>G
NG_066624.1:g.430300T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4941T>G	ENSP00000055163.8:p.Ser1647=
ENST00000414678.8:c.5010T>G	ENSP00000412835.3:p.Ser1670=
ENST00000637015.2:c.5229T>G	ENSP00000489729.2:p.Ser1743=
ENST00000346085.10:c.4980T>G	ENSP00000344546.5:p.Ser1660=
ENST00000350026.10:c.4692T>G	ENSP00000055163.7:p.Ser1564=
ENST00000414678.7:c.3258T>G	ENSP00000412835.2:p.Ser1086=
ENST00000635849.1:c.2421T>G	ENSP00000490948.1:p.Ser807=
ENST00000635957.1:c.2052T>G	ENSP00000490385.1:p.Ser684=
ENST00000636227.1:n.3563T>G
ENST00000636254.1:n.1020T>G
ENST00000636930.2:c.5100T>G MANE Select	ENSP00000490491.2:p.Ser1700=
ENST00000636940.1:n.3097T>G
ENST00000637015.1:c.2468T>G
ENST00000637568.1:c.2382T>G
ENST00000637741.1:n.1766T>G
ENST00000637810.1:c.2442T>G	ENSP00000489636.1:p.Ser814=
ENST00000637904.1:c.2601T>G	ENSP00000490550.1:p.Ser867=
ENST00000647938.1:c.4731T>G	ENSP00000498155.1:p.Ser1577=
ENST00000346085.9:c.4731T>G	ENSP00000344546.4:p.Ser1577=
ENST00000350026.9:c.4692T>G	ENSP00000055163.7:p.Ser1564=
ENST00000414678.6:c.3258T>G	ENSP00000412835.2:p.Ser1086=
NM_017519.2:c.4692T>G	NP_059989.2:p.Ser1564=
NM_020732.3:c.4731T>G	NP_065783.3:p.Ser1577=
XM_005267069.3:c.4851T>G	XP_005267126.2:p.Ser1617=
XM_011535984.1:c.3930T>G	XP_011534286.1:p.Ser1310=
XM_011535985.1:c.3750T>G	XP_011534287.1:p.Ser1250=
XM_011535986.1:c.3510T>G	XP_011534288.1:p.Ser1170=
XM_011535987.1:c.3129T>G	XP_011534289.1:p.Ser1043=
XM_011535988.1:c.1992T>G	XP_011534290.1:p.Ser664=
NM_001346813.1:c.4851T>G	NP_001333742.1:p.Ser1617=
NM_001363725.1:c.2601T>G	NP_001350654.1:p.Ser867=
XM_011535984.2:c.5061T>G	XP_011534286.2:p.Ser1687=
XM_011535988.3:c.1992T>G	XP_011534290.1:p.Ser664=
XM_017011103.2:c.4962T>G	XP_016866592.1:p.Ser1654=
XM_017011104.1:c.4932T>G	XP_016866593.1:p.Ser1644=
XM_017011105.2:c.4902T>G	XP_016866594.1:p.Ser1634=
XM_017011106.2:c.4773T>G	XP_016866595.1:p.Ser1591=
XM_017011107.2:c.4752T>G	XP_016866596.1:p.Ser1584=
XR_002956289.1:n.5047T>G
NM_001363725.2:c.2601T>G	NP_001350654.1:p.Ser867=
NM_001371656.1:c.4980T>G	NP_001358585.1:p.Ser1660=
NM_001374820.1:c.4980T>G	NP_001361749.1:p.Ser1660=
NM_001374828.1:c.5100T>G MANE Select	NP_001361757.1:p.Ser1700=
NM_017519.3:c.4941T>G	NP_059989.3:p.Ser1647=