Canonical Allele Identifier: CA366239515

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157519957T>A (hg19) ; chr6:g.157198823T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198823T>A , CM000668.2:g.157198823T>A	GRCh38
NC_000006.11:g.157519957T>A , CM000668.1:g.157519957T>A	GRCh37
NC_000006.10:g.157561649T>A	NCBI36
NG_032093.1:g.425894T>A
NG_032093.2:g.425894T>A
NG_066624.1:g.427798T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4236T>A	ENSP00000055163.8:p.Tyr1412Ter
ENST00000414678.8:c.4305T>A	ENSP00000412835.3:p.Tyr1435Ter
ENST00000637015.2:c.4524T>A	ENSP00000489729.2:p.Tyr1508Ter
ENST00000346085.10:c.4275T>A	ENSP00000344546.5:p.Tyr1425Ter
ENST00000350026.10:c.3987T>A	ENSP00000055163.7:p.Tyr1329Ter
ENST00000414678.7:c.2553T>A	ENSP00000412835.2:p.Tyr851Ter
ENST00000635849.1:c.1716T>A	ENSP00000490948.1:p.Tyr572Ter
ENST00000635957.1:c.1347T>A	ENSP00000490385.1:p.Tyr449Ter
ENST00000636227.1:n.2858T>A
ENST00000636254.1:n.315T>A
ENST00000636930.2:c.4395T>A MANE Select	ENSP00000490491.2:p.Tyr1465Ter
ENST00000636940.1:n.2392T>A
ENST00000637015.1:c.1763T>A
ENST00000637568.1:c.1677T>A
ENST00000637741.1:n.1061T>A
ENST00000637810.1:c.1737T>A	ENSP00000489636.1:p.Tyr579Ter
ENST00000637904.1:c.1896T>A	ENSP00000490550.1:p.Tyr632Ter
ENST00000647938.1:c.4026T>A	ENSP00000498155.1:p.Tyr1342Ter
ENST00000346085.9:c.4026T>A	ENSP00000344546.4:p.Tyr1342Ter
ENST00000350026.9:c.3987T>A	ENSP00000055163.7:p.Tyr1329Ter
ENST00000414678.6:c.2553T>A	ENSP00000412835.2:p.Tyr851Ter
NM_017519.2:c.3987T>A	NP_059989.2:p.Tyr1329Ter
NM_020732.3:c.4026T>A	NP_065783.3:p.Tyr1342Ter
XM_005267069.3:c.4146T>A	XP_005267126.2:p.Tyr1382Ter
XM_011535984.1:c.3225T>A	XP_011534286.1:p.Tyr1075Ter
XM_011535985.1:c.3045T>A	XP_011534287.1:p.Tyr1015Ter
XM_011535986.1:c.2805T>A	XP_011534288.1:p.Tyr935Ter
XM_011535987.1:c.2424T>A	XP_011534289.1:p.Tyr808Ter
XM_011535988.1:c.1287T>A	XP_011534290.1:p.Tyr429Ter
NM_001346813.1:c.4146T>A	NP_001333742.1:p.Tyr1382Ter
NM_001363725.1:c.1896T>A	NP_001350654.1:p.Tyr632Ter
XM_011535984.2:c.4356T>A	XP_011534286.2:p.Tyr1452Ter
XM_011535988.3:c.1287T>A	XP_011534290.1:p.Tyr429Ter
XM_017011103.2:c.4257T>A	XP_016866592.1:p.Tyr1419Ter
XM_017011104.1:c.4227T>A	XP_016866593.1:p.Tyr1409Ter
XM_017011105.2:c.4197T>A	XP_016866594.1:p.Tyr1399Ter
XM_017011106.2:c.4068T>A	XP_016866595.1:p.Tyr1356Ter
XM_017011107.2:c.4047T>A	XP_016866596.1:p.Tyr1349Ter
XR_002956289.1:n.4427-1882T>A
NM_001363725.2:c.1896T>A	NP_001350654.1:p.Tyr632Ter
NM_001371656.1:c.4275T>A	NP_001358585.1:p.Tyr1425Ter
NM_001374820.1:c.4275T>A	NP_001361749.1:p.Tyr1425Ter
NM_001374828.1:c.4395T>A MANE Select	NP_001361757.1:p.Tyr1465Ter
NM_017519.3:c.4236T>A	NP_059989.3:p.Tyr1412Ter