Canonical Allele Identifier: CA452781519

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128338814
• gnomAD v4: 6-157189691-C-T
• MyVariant Identifiers: chr6:g.157510825C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189691C>T , CM000668.2:g.157189691C>T	GRCh38
NC_000006.11:g.157510825C>T , CM000668.1:g.157510825C>T	GRCh37
NC_000006.10:g.157552517C>T	NCBI36
NG_032093.1:g.416762C>T
NG_032093.2:g.416762C>T
NG_066624.1:g.418666C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3810C>T	ENSP00000055163.8:p.Ser1270=
ENST00000414678.8:c.3879C>T	ENSP00000412835.3:p.Ser1293=
ENST00000637015.2:c.4098C>T	ENSP00000489729.2:p.Ser1366=
ENST00000346085.10:c.3849C>T	ENSP00000344546.5:p.Ser1283=
ENST00000350026.10:c.3561C>T	ENSP00000055163.7:p.Ser1187=
ENST00000414678.7:c.2127C>T	ENSP00000412835.2:p.Ser709=
ENST00000635849.1:c.1290C>T	ENSP00000490948.1:p.Ser430=
ENST00000635957.1:c.924C>T	ENSP00000490385.1:p.Ser308=
ENST00000636930.2:c.3969C>T MANE Select	ENSP00000490491.2:p.Ser1323=
ENST00000636940.1:n.1966C>T
ENST00000637015.1:c.1337C>T
ENST00000637568.1:c.1251C>T
ENST00000637741.1:n.635C>T
ENST00000637810.1:c.1311C>T	ENSP00000489636.1:p.Ser437=
ENST00000637904.1:c.1470C>T	ENSP00000490550.1:p.Ser490=
ENST00000647938.1:c.3600C>T	ENSP00000498155.1:p.Ser1200=
ENST00000346085.9:c.3600C>T	ENSP00000344546.4:p.Ser1200=
ENST00000350026.9:c.3561C>T	ENSP00000055163.7:p.Ser1187=
ENST00000414678.6:c.2127C>T	ENSP00000412835.2:p.Ser709=
NM_017519.2:c.3561C>T	NP_059989.2:p.Ser1187=
NM_020732.3:c.3600C>T	NP_065783.3:p.Ser1200=
XM_005267069.3:c.3720C>T	XP_005267126.2:p.Ser1240=
XM_011535984.1:c.2799C>T	XP_011534286.1:p.Ser933=
XM_011535985.1:c.2619C>T	XP_011534287.1:p.Ser873=
XM_011535986.1:c.2379C>T	XP_011534288.1:p.Ser793=
XM_011535987.1:c.1998C>T	XP_011534289.1:p.Ser666=
XM_011535988.1:c.861C>T	XP_011534290.1:p.Ser287=
NM_001346813.1:c.3720C>T	NP_001333742.1:p.Ser1240=
NM_001363725.1:c.1470C>T	NP_001350654.1:p.Ser490=
XM_011535984.2:c.3930C>T	XP_011534286.2:p.Ser1310=
XM_011535988.3:c.861C>T	XP_011534290.1:p.Ser287=
XM_017011103.2:c.3831C>T	XP_016866592.1:p.Ser1277=
XM_017011104.1:c.3801C>T	XP_016866593.1:p.Ser1267=
XM_017011105.2:c.3771C>T	XP_016866594.1:p.Ser1257=
XM_017011106.2:c.3642C>T	XP_016866595.1:p.Ser1214=
XM_017011107.2:c.3621C>T	XP_016866596.1:p.Ser1207=
XR_002956289.1:n.4013C>T
NM_001363725.2:c.1470C>T	NP_001350654.1:p.Ser490=
NM_001371656.1:c.3849C>T	NP_001358585.1:p.Ser1283=
NM_001374820.1:c.3849C>T	NP_001361749.1:p.Ser1283=
NM_001374828.1:c.3969C>T MANE Select	NP_001361757.1:p.Ser1323=
NM_017519.3:c.3810C>T	NP_059989.3:p.Ser1270=