Canonical Allele Identifier: CA452781558

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157189742-C-T
• MyVariant Identifiers: chr6:g.157510876C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189742C>T , CM000668.2:g.157189742C>T	GRCh38
NC_000006.11:g.157510876C>T , CM000668.1:g.157510876C>T	GRCh37
NC_000006.10:g.157552568C>T	NCBI36
NG_032093.1:g.416813C>T
NG_032093.2:g.416813C>T
NG_066624.1:g.418717C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3861C>T	ENSP00000055163.8:p.Ser1287=
ENST00000414678.8:c.3930C>T	ENSP00000412835.3:p.Ser1310=
ENST00000637015.2:c.4149C>T	ENSP00000489729.2:p.Ser1383=
ENST00000346085.10:c.3900C>T	ENSP00000344546.5:p.Ser1300=
ENST00000350026.10:c.3612C>T	ENSP00000055163.7:p.Ser1204=
ENST00000414678.7:c.2178C>T	ENSP00000412835.2:p.Ser726=
ENST00000635849.1:c.1341C>T	ENSP00000490948.1:p.Ser447=
ENST00000635957.1:c.975C>T	ENSP00000490385.1:p.Ser325=
ENST00000636930.2:c.4020C>T MANE Select	ENSP00000490491.2:p.Ser1340=
ENST00000636940.1:n.2017C>T
ENST00000637015.1:c.1388C>T
ENST00000637568.1:c.1302C>T
ENST00000637741.1:n.686C>T
ENST00000637810.1:c.1362C>T	ENSP00000489636.1:p.Ser454=
ENST00000637904.1:c.1521C>T	ENSP00000490550.1:p.Ser507=
ENST00000647938.1:c.3651C>T	ENSP00000498155.1:p.Ser1217=
ENST00000346085.9:c.3651C>T	ENSP00000344546.4:p.Ser1217=
ENST00000350026.9:c.3612C>T	ENSP00000055163.7:p.Ser1204=
ENST00000414678.6:c.2178C>T	ENSP00000412835.2:p.Ser726=
NM_017519.2:c.3612C>T	NP_059989.2:p.Ser1204=
NM_020732.3:c.3651C>T	NP_065783.3:p.Ser1217=
XM_005267069.3:c.3771C>T	XP_005267126.2:p.Ser1257=
XM_011535984.1:c.2850C>T	XP_011534286.1:p.Ser950=
XM_011535985.1:c.2670C>T	XP_011534287.1:p.Ser890=
XM_011535986.1:c.2430C>T	XP_011534288.1:p.Ser810=
XM_011535987.1:c.2049C>T	XP_011534289.1:p.Ser683=
XM_011535988.1:c.912C>T	XP_011534290.1:p.Ser304=
NM_001346813.1:c.3771C>T	NP_001333742.1:p.Ser1257=
NM_001363725.1:c.1521C>T	NP_001350654.1:p.Ser507=
XM_011535984.2:c.3981C>T	XP_011534286.2:p.Ser1327=
XM_011535988.3:c.912C>T	XP_011534290.1:p.Ser304=
XM_017011103.2:c.3882C>T	XP_016866592.1:p.Ser1294=
XM_017011104.1:c.3852C>T	XP_016866593.1:p.Ser1284=
XM_017011105.2:c.3822C>T	XP_016866594.1:p.Ser1274=
XM_017011106.2:c.3693C>T	XP_016866595.1:p.Ser1231=
XM_017011107.2:c.3672C>T	XP_016866596.1:p.Ser1224=
XR_002956289.1:n.4064C>T
NM_001363725.2:c.1521C>T	NP_001350654.1:p.Ser507=
NM_001371656.1:c.3900C>T	NP_001358585.1:p.Ser1300=
NM_001374820.1:c.3900C>T	NP_001361749.1:p.Ser1300=
NM_001374828.1:c.4020C>T MANE Select	NP_001361757.1:p.Ser1340=
NM_017519.3:c.3861C>T	NP_059989.3:p.Ser1287=