Canonical Allele Identifier: CA366238339

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157196232C>A , CM000668.2:g.157196232C>A	GRCh38
NC_000006.11:g.157517366C>A , CM000668.1:g.157517366C>A	GRCh37
NC_000006.10:g.157559058C>A	NCBI36
NG_032093.1:g.423303C>A
NG_032093.2:g.423303C>A
NG_066624.1:g.425207C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4299C>A MANE Select	NP_001361757.1:p.Tyr1433Ter
ENST00000636930.2:c.4299C>A MANE Select	ENSP00000490491.2:p.Tyr1433Ter
NM_001346813.1:c.4050C>A	NP_001333742.1:p.Tyr1350Ter
NM_001363725.1:c.1800C>A	NP_001350654.1:p.Tyr600Ter
NM_001363725.2:c.1800C>A	NP_001350654.1:p.Tyr600Ter
NM_001371656.1:c.4179C>A	NP_001358585.1:p.Tyr1393Ter
NM_001374820.1:c.4179C>A	NP_001361749.1:p.Tyr1393Ter
NM_017519.2:c.3891C>A	NP_059989.2:p.Tyr1297Ter
NM_017519.3:c.4140C>A	NP_059989.3:p.Tyr1380Ter
NM_020732.3:c.3930C>A	NP_065783.3:p.Tyr1310Ter
ENST00000346085.10:c.4179C>A	ENSP00000344546.5:p.Tyr1393Ter
ENST00000346085.9:c.3930C>A	ENSP00000344546.4:p.Tyr1310Ter
ENST00000350026.10:c.3891C>A	ENSP00000055163.7:p.Tyr1297Ter
ENST00000350026.11:c.4140C>A	ENSP00000055163.8:p.Tyr1380Ter
ENST00000350026.9:c.3891C>A	ENSP00000055163.7:p.Tyr1297Ter
ENST00000414678.6:c.2457C>A	ENSP00000412835.2:p.Tyr819Ter
ENST00000414678.7:c.2457C>A	ENSP00000412835.2:p.Tyr819Ter
ENST00000414678.8:c.4209C>A	ENSP00000412835.3:p.Tyr1403Ter
ENST00000635849.1:c.1620C>A	ENSP00000490948.1:p.Tyr540Ter
ENST00000635957.1:c.1251C>A	ENSP00000490385.1:p.Tyr417Ter
ENST00000636227.1:n.2762C>A
ENST00000636940.1:n.2296C>A
ENST00000637015.1:c.1667C>A
ENST00000637015.2:c.4428C>A	ENSP00000489729.2:p.Tyr1476Ter
ENST00000637568.1:c.1581C>A
ENST00000637741.1:n.965C>A
ENST00000637810.1:c.1641C>A	ENSP00000489636.1:p.Tyr547Ter
ENST00000637904.1:c.1800C>A	ENSP00000490550.1:p.Tyr600Ter
ENST00000647938.1:c.3930C>A	ENSP00000498155.1:p.Tyr1310Ter
XM_005267069.3:c.4050C>A	XP_005267126.2:p.Tyr1350Ter
XM_011535984.1:c.3129C>A	XP_011534286.1:p.Tyr1043Ter
XM_011535984.2:c.4260C>A	XP_011534286.2:p.Tyr1420Ter
XM_011535985.1:c.2949C>A	XP_011534287.1:p.Tyr983Ter
XM_011535986.1:c.2709C>A	XP_011534288.1:p.Tyr903Ter
XM_011535987.1:c.2328C>A	XP_011534289.1:p.Tyr776Ter
XM_011535988.1:c.1191C>A	XP_011534290.1:p.Tyr397Ter
XM_011535988.3:c.1191C>A	XP_011534290.1:p.Tyr397Ter
XM_017011103.2:c.4161C>A	XP_016866592.1:p.Tyr1387Ter
XM_017011104.1:c.4131C>A	XP_016866593.1:p.Tyr1377Ter
XM_017011105.2:c.4101C>A	XP_016866594.1:p.Tyr1367Ter
XM_017011106.2:c.3972C>A	XP_016866595.1:p.Tyr1324Ter
XM_017011107.2:c.3951C>A	XP_016866596.1:p.Tyr1317Ter
XR_002956289.1:n.4343C>A