Canonical Allele Identifier: CA366234151

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510850G>T (hg19) ; chr6:g.157189716G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189716G>T , CM000668.2:g.157189716G>T	GRCh38
NC_000006.11:g.157510850G>T , CM000668.1:g.157510850G>T	GRCh37
NC_000006.10:g.157552542G>T	NCBI36
NG_032093.1:g.416787G>T
NG_032093.2:g.416787G>T
NG_066624.1:g.418691G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3835G>T	ENSP00000055163.8:p.Asp1279Tyr
ENST00000414678.8:c.3904G>T	ENSP00000412835.3:p.Asp1302Tyr
ENST00000637015.2:c.4123G>T	ENSP00000489729.2:p.Asp1375Tyr
ENST00000346085.10:c.3874G>T	ENSP00000344546.5:p.Asp1292Tyr
ENST00000350026.10:c.3586G>T	ENSP00000055163.7:p.Asp1196Tyr
ENST00000414678.7:c.2152G>T	ENSP00000412835.2:p.Asp718Tyr
ENST00000635849.1:c.1315G>T	ENSP00000490948.1:p.Asp439Tyr
ENST00000635957.1:c.949G>T	ENSP00000490385.1:p.Asp317Tyr
ENST00000636930.2:c.3994G>T MANE Select	ENSP00000490491.2:p.Asp1332Tyr
ENST00000636940.1:n.1991G>T
ENST00000637015.1:c.1362G>T
ENST00000637568.1:c.1276G>T
ENST00000637741.1:n.660G>T
ENST00000637810.1:c.1336G>T	ENSP00000489636.1:p.Asp446Tyr
ENST00000637904.1:c.1495G>T	ENSP00000490550.1:p.Asp499Tyr
ENST00000647938.1:c.3625G>T	ENSP00000498155.1:p.Asp1209Tyr
ENST00000346085.9:c.3625G>T	ENSP00000344546.4:p.Asp1209Tyr
ENST00000350026.9:c.3586G>T	ENSP00000055163.7:p.Asp1196Tyr
ENST00000414678.6:c.2152G>T	ENSP00000412835.2:p.Asp718Tyr
NM_017519.2:c.3586G>T	NP_059989.2:p.Asp1196Tyr
NM_020732.3:c.3625G>T	NP_065783.3:p.Asp1209Tyr
XM_005267069.3:c.3745G>T	XP_005267126.2:p.Asp1249Tyr
XM_011535984.1:c.2824G>T	XP_011534286.1:p.Asp942Tyr
XM_011535985.1:c.2644G>T	XP_011534287.1:p.Asp882Tyr
XM_011535986.1:c.2404G>T	XP_011534288.1:p.Asp802Tyr
XM_011535987.1:c.2023G>T	XP_011534289.1:p.Asp675Tyr
XM_011535988.1:c.886G>T	XP_011534290.1:p.Asp296Tyr
NM_001346813.1:c.3745G>T	NP_001333742.1:p.Asp1249Tyr
NM_001363725.1:c.1495G>T	NP_001350654.1:p.Asp499Tyr
XM_011535984.2:c.3955G>T	XP_011534286.2:p.Asp1319Tyr
XM_011535988.3:c.886G>T	XP_011534290.1:p.Asp296Tyr
XM_017011103.2:c.3856G>T	XP_016866592.1:p.Asp1286Tyr
XM_017011104.1:c.3826G>T	XP_016866593.1:p.Asp1276Tyr
XM_017011105.2:c.3796G>T	XP_016866594.1:p.Asp1266Tyr
XM_017011106.2:c.3667G>T	XP_016866595.1:p.Asp1223Tyr
XM_017011107.2:c.3646G>T	XP_016866596.1:p.Asp1216Tyr
XR_002956289.1:n.4038G>T
NM_001363725.2:c.1495G>T	NP_001350654.1:p.Asp499Tyr
NM_001371656.1:c.3874G>T	NP_001358585.1:p.Asp1292Tyr
NM_001374820.1:c.3874G>T	NP_001361749.1:p.Asp1292Tyr
NM_001374828.1:c.3994G>T MANE Select	NP_001361757.1:p.Asp1332Tyr
NM_017519.3:c.3835G>T	NP_059989.3:p.Asp1279Tyr