Canonical Allele Identifier: CA452781909

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190122-C-A
• MyVariant Identifiers: chr6:g.157511256C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190122C>A , CM000668.2:g.157190122C>A	GRCh38
NC_000006.11:g.157511256C>A , CM000668.1:g.157511256C>A	GRCh37
NC_000006.10:g.157552948C>A	NCBI36
NG_032093.1:g.417193C>A
NG_032093.2:g.417193C>A
NG_066624.1:g.419097C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3984C>A	ENSP00000055163.8:p.Ala1328=
ENST00000414678.8:c.4053C>A	ENSP00000412835.3:p.Ala1351=
ENST00000637015.2:c.4272C>A	ENSP00000489729.2:p.Ala1424=
ENST00000346085.10:c.4023C>A	ENSP00000344546.5:p.Ala1341=
ENST00000350026.10:c.3735C>A	ENSP00000055163.7:p.Ala1245=
ENST00000414678.7:c.2301C>A	ENSP00000412835.2:p.Ala767=
ENST00000635849.1:c.1464C>A	ENSP00000490948.1:p.Ala488=
ENST00000635957.1:c.1095C>A	ENSP00000490385.1:p.Ala365=
ENST00000636930.2:c.4143C>A MANE Select	ENSP00000490491.2:p.Ala1381=
ENST00000636940.1:n.2140C>A
ENST00000637015.1:c.1511C>A
ENST00000637568.1:c.1425C>A
ENST00000637741.1:n.809C>A
ENST00000637810.1:c.1485C>A	ENSP00000489636.1:p.Ala495=
ENST00000637904.1:c.1644C>A	ENSP00000490550.1:p.Ala548=
ENST00000647938.1:c.3774C>A	ENSP00000498155.1:p.Ala1258=
ENST00000346085.9:c.3774C>A	ENSP00000344546.4:p.Ala1258=
ENST00000350026.9:c.3735C>A	ENSP00000055163.7:p.Ala1245=
ENST00000414678.6:c.2301C>A	ENSP00000412835.2:p.Ala767=
NM_017519.2:c.3735C>A	NP_059989.2:p.Ala1245=
NM_020732.3:c.3774C>A	NP_065783.3:p.Ala1258=
XM_005267069.3:c.3894C>A	XP_005267126.2:p.Ala1298=
XM_011535984.1:c.2973C>A	XP_011534286.1:p.Ala991=
XM_011535985.1:c.2793C>A	XP_011534287.1:p.Ala931=
XM_011535986.1:c.2553C>A	XP_011534288.1:p.Ala851=
XM_011535987.1:c.2172C>A	XP_011534289.1:p.Ala724=
XM_011535988.1:c.1035C>A	XP_011534290.1:p.Ala345=
NM_001346813.1:c.3894C>A	NP_001333742.1:p.Ala1298=
NM_001363725.1:c.1644C>A	NP_001350654.1:p.Ala548=
XM_011535984.2:c.4104C>A	XP_011534286.2:p.Ala1368=
XM_011535988.3:c.1035C>A	XP_011534290.1:p.Ala345=
XM_017011103.2:c.4005C>A	XP_016866592.1:p.Ala1335=
XM_017011104.1:c.3975C>A	XP_016866593.1:p.Ala1325=
XM_017011105.2:c.3945C>A	XP_016866594.1:p.Ala1315=
XM_017011106.2:c.3816C>A	XP_016866595.1:p.Ala1272=
XM_017011107.2:c.3795C>A	XP_016866596.1:p.Ala1265=
XR_002956289.1:n.4187C>A
NM_001363725.2:c.1644C>A	NP_001350654.1:p.Ala548=
NM_001371656.1:c.4023C>A	NP_001358585.1:p.Ala1341=
NM_001374820.1:c.4023C>A	NP_001361749.1:p.Ala1341=
NM_001374828.1:c.4143C>A MANE Select	NP_001361757.1:p.Ala1381=
NM_017519.3:c.3984C>A	NP_059989.3:p.Ala1328=