Canonical Allele Identifier: CA366235294

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190111-A-G
• MyVariant Identifiers: chr6:g.157511245A>G (hg19) ; chr6:g.157190111A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190111A>G , CM000668.2:g.157190111A>G	GRCh38
NC_000006.11:g.157511245A>G , CM000668.1:g.157511245A>G	GRCh37
NC_000006.10:g.157552937A>G	NCBI36
NG_032093.1:g.417182A>G
NG_032093.2:g.417182A>G
NG_066624.1:g.419086A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3973A>G	ENSP00000055163.8:p.Thr1325Ala
ENST00000414678.8:c.4042A>G	ENSP00000412835.3:p.Thr1348Ala
ENST00000637015.2:c.4261A>G	ENSP00000489729.2:p.Thr1421Ala
ENST00000346085.10:c.4012A>G	ENSP00000344546.5:p.Thr1338Ala
ENST00000350026.10:c.3724A>G	ENSP00000055163.7:p.Thr1242Ala
ENST00000414678.7:c.2290A>G	ENSP00000412835.2:p.Thr764Ala
ENST00000635849.1:c.1453A>G	ENSP00000490948.1:p.Thr485Ala
ENST00000635957.1:c.1084A>G	ENSP00000490385.1:p.Thr362Ala
ENST00000636930.2:c.4132A>G MANE Select	ENSP00000490491.2:p.Thr1378Ala
ENST00000636940.1:n.2129A>G
ENST00000637015.1:c.1500A>G
ENST00000637568.1:c.1414A>G
ENST00000637741.1:n.798A>G
ENST00000637810.1:c.1474A>G	ENSP00000489636.1:p.Thr492Ala
ENST00000637904.1:c.1633A>G	ENSP00000490550.1:p.Thr545Ala
ENST00000647938.1:c.3763A>G	ENSP00000498155.1:p.Thr1255Ala
ENST00000346085.9:c.3763A>G	ENSP00000344546.4:p.Thr1255Ala
ENST00000350026.9:c.3724A>G	ENSP00000055163.7:p.Thr1242Ala
ENST00000414678.6:c.2290A>G	ENSP00000412835.2:p.Thr764Ala
NM_017519.2:c.3724A>G	NP_059989.2:p.Thr1242Ala
NM_020732.3:c.3763A>G	NP_065783.3:p.Thr1255Ala
XM_005267069.3:c.3883A>G	XP_005267126.2:p.Thr1295Ala
XM_011535984.1:c.2962A>G	XP_011534286.1:p.Thr988Ala
XM_011535985.1:c.2782A>G	XP_011534287.1:p.Thr928Ala
XM_011535986.1:c.2542A>G	XP_011534288.1:p.Thr848Ala
XM_011535987.1:c.2161A>G	XP_011534289.1:p.Thr721Ala
XM_011535988.1:c.1024A>G	XP_011534290.1:p.Thr342Ala
NM_001346813.1:c.3883A>G	NP_001333742.1:p.Thr1295Ala
NM_001363725.1:c.1633A>G	NP_001350654.1:p.Thr545Ala
XM_011535984.2:c.4093A>G	XP_011534286.2:p.Thr1365Ala
XM_011535988.3:c.1024A>G	XP_011534290.1:p.Thr342Ala
XM_017011103.2:c.3994A>G	XP_016866592.1:p.Thr1332Ala
XM_017011104.1:c.3964A>G	XP_016866593.1:p.Thr1322Ala
XM_017011105.2:c.3934A>G	XP_016866594.1:p.Thr1312Ala
XM_017011106.2:c.3805A>G	XP_016866595.1:p.Thr1269Ala
XM_017011107.2:c.3784A>G	XP_016866596.1:p.Thr1262Ala
XR_002956289.1:n.4176A>G
NM_001363725.2:c.1633A>G	NP_001350654.1:p.Thr545Ala
NM_001371656.1:c.4012A>G	NP_001358585.1:p.Thr1338Ala
NM_001374820.1:c.4012A>G	NP_001361749.1:p.Thr1338Ala
NM_001374828.1:c.4132A>G MANE Select	NP_001361757.1:p.Thr1378Ala
NM_017519.3:c.3973A>G	NP_059989.3:p.Thr1325Ala