Canonical Allele Identifier: CA452781539

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157189721-G-A
• MyVariant Identifiers: chr6:g.157510855G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189721G>A , CM000668.2:g.157189721G>A	GRCh38
NC_000006.11:g.157510855G>A , CM000668.1:g.157510855G>A	GRCh37
NC_000006.10:g.157552547G>A	NCBI36
NG_032093.1:g.416792G>A
NG_032093.2:g.416792G>A
NG_066624.1:g.418696G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3840G>A	ENSP00000055163.8:p.Leu1280=
ENST00000414678.8:c.3909G>A	ENSP00000412835.3:p.Leu1303=
ENST00000637015.2:c.4128G>A	ENSP00000489729.2:p.Leu1376=
ENST00000346085.10:c.3879G>A	ENSP00000344546.5:p.Leu1293=
ENST00000350026.10:c.3591G>A	ENSP00000055163.7:p.Leu1197=
ENST00000414678.7:c.2157G>A	ENSP00000412835.2:p.Leu719=
ENST00000635849.1:c.1320G>A	ENSP00000490948.1:p.Leu440=
ENST00000635957.1:c.954G>A	ENSP00000490385.1:p.Leu318=
ENST00000636930.2:c.3999G>A MANE Select	ENSP00000490491.2:p.Leu1333=
ENST00000636940.1:n.1996G>A
ENST00000637015.1:c.1367G>A
ENST00000637568.1:c.1281G>A
ENST00000637741.1:n.665G>A
ENST00000637810.1:c.1341G>A	ENSP00000489636.1:p.Leu447=
ENST00000637904.1:c.1500G>A	ENSP00000490550.1:p.Leu500=
ENST00000647938.1:c.3630G>A	ENSP00000498155.1:p.Leu1210=
ENST00000346085.9:c.3630G>A	ENSP00000344546.4:p.Leu1210=
ENST00000350026.9:c.3591G>A	ENSP00000055163.7:p.Leu1197=
ENST00000414678.6:c.2157G>A	ENSP00000412835.2:p.Leu719=
NM_017519.2:c.3591G>A	NP_059989.2:p.Leu1197=
NM_020732.3:c.3630G>A	NP_065783.3:p.Leu1210=
XM_005267069.3:c.3750G>A	XP_005267126.2:p.Leu1250=
XM_011535984.1:c.2829G>A	XP_011534286.1:p.Leu943=
XM_011535985.1:c.2649G>A	XP_011534287.1:p.Leu883=
XM_011535986.1:c.2409G>A	XP_011534288.1:p.Leu803=
XM_011535987.1:c.2028G>A	XP_011534289.1:p.Leu676=
XM_011535988.1:c.891G>A	XP_011534290.1:p.Leu297=
NM_001346813.1:c.3750G>A	NP_001333742.1:p.Leu1250=
NM_001363725.1:c.1500G>A	NP_001350654.1:p.Leu500=
XM_011535984.2:c.3960G>A	XP_011534286.2:p.Leu1320=
XM_011535988.3:c.891G>A	XP_011534290.1:p.Leu297=
XM_017011103.2:c.3861G>A	XP_016866592.1:p.Leu1287=
XM_017011104.1:c.3831G>A	XP_016866593.1:p.Leu1277=
XM_017011105.2:c.3801G>A	XP_016866594.1:p.Leu1267=
XM_017011106.2:c.3672G>A	XP_016866595.1:p.Leu1224=
XM_017011107.2:c.3651G>A	XP_016866596.1:p.Leu1217=
XR_002956289.1:n.4043G>A
NM_001363725.2:c.1500G>A	NP_001350654.1:p.Leu500=
NM_001371656.1:c.3879G>A	NP_001358585.1:p.Leu1293=
NM_001374820.1:c.3879G>A	NP_001361749.1:p.Leu1293=
NM_001374828.1:c.3999G>A MANE Select	NP_001361757.1:p.Leu1333=
NM_017519.3:c.3840G>A	NP_059989.3:p.Leu1280=