Canonical Allele Identifier: CA452783934

Gene: ARID1B

Linked Data

• dbSNP Id: rs1461804390
• MyVariant Identifiers: chr6:g.157519981C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198847C>T , CM000668.2:g.157198847C>T	GRCh38
NC_000006.11:g.157519981C>T , CM000668.1:g.157519981C>T	GRCh37
NC_000006.10:g.157561673C>T	NCBI36
NG_032093.1:g.425918C>T
NG_032093.2:g.425918C>T
NG_066624.1:g.427822C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4260C>T	ENSP00000055163.8:p.Gly1420=
ENST00000414678.8:c.4329C>T	ENSP00000412835.3:p.Gly1443=
ENST00000637015.2:c.4548C>T	ENSP00000489729.2:p.Gly1516=
ENST00000346085.10:c.4299C>T	ENSP00000344546.5:p.Gly1433=
ENST00000350026.10:c.4011C>T	ENSP00000055163.7:p.Gly1337=
ENST00000414678.7:c.2577C>T	ENSP00000412835.2:p.Gly859=
ENST00000635849.1:c.1740C>T	ENSP00000490948.1:p.Gly580=
ENST00000635957.1:c.1371C>T	ENSP00000490385.1:p.Gly457=
ENST00000636227.1:n.2882C>T
ENST00000636254.1:n.339C>T
ENST00000636930.2:c.4419C>T MANE Select	ENSP00000490491.2:p.Gly1473=
ENST00000636940.1:n.2416C>T
ENST00000637015.1:c.1787C>T
ENST00000637568.1:c.1701C>T
ENST00000637741.1:n.1085C>T
ENST00000637810.1:c.1761C>T	ENSP00000489636.1:p.Gly587=
ENST00000637904.1:c.1920C>T	ENSP00000490550.1:p.Gly640=
ENST00000647938.1:c.4050C>T	ENSP00000498155.1:p.Gly1350=
ENST00000346085.9:c.4050C>T	ENSP00000344546.4:p.Gly1350=
ENST00000350026.9:c.4011C>T	ENSP00000055163.7:p.Gly1337=
ENST00000414678.6:c.2577C>T	ENSP00000412835.2:p.Gly859=
NM_017519.2:c.4011C>T	NP_059989.2:p.Gly1337=
NM_020732.3:c.4050C>T	NP_065783.3:p.Gly1350=
XM_005267069.3:c.4170C>T	XP_005267126.2:p.Gly1390=
XM_011535984.1:c.3249C>T	XP_011534286.1:p.Gly1083=
XM_011535985.1:c.3069C>T	XP_011534287.1:p.Gly1023=
XM_011535986.1:c.2829C>T	XP_011534288.1:p.Gly943=
XM_011535987.1:c.2448C>T	XP_011534289.1:p.Gly816=
XM_011535988.1:c.1311C>T	XP_011534290.1:p.Gly437=
NM_001346813.1:c.4170C>T	NP_001333742.1:p.Gly1390=
NM_001363725.1:c.1920C>T	NP_001350654.1:p.Gly640=
XM_011535984.2:c.4380C>T	XP_011534286.2:p.Gly1460=
XM_011535988.3:c.1311C>T	XP_011534290.1:p.Gly437=
XM_017011103.2:c.4281C>T	XP_016866592.1:p.Gly1427=
XM_017011104.1:c.4251C>T	XP_016866593.1:p.Gly1417=
XM_017011105.2:c.4221C>T	XP_016866594.1:p.Gly1407=
XM_017011106.2:c.4092C>T	XP_016866595.1:p.Gly1364=
XM_017011107.2:c.4071C>T	XP_016866596.1:p.Gly1357=
XR_002956289.1:n.4427-1858C>T
NM_001363725.2:c.1920C>T	NP_001350654.1:p.Gly640=
NM_001371656.1:c.4299C>T	NP_001358585.1:p.Gly1433=
NM_001374820.1:c.4299C>T	NP_001361749.1:p.Gly1433=
NM_001374828.1:c.4419C>T MANE Select	NP_001361757.1:p.Gly1473=
NM_017519.3:c.4260C>T	NP_059989.3:p.Gly1420=