Canonical Allele Identifier: CA366234067

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510812A>T (hg19) ; chr6:g.157189678A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189678A>T , CM000668.2:g.157189678A>T	GRCh38
NC_000006.11:g.157510812A>T , CM000668.1:g.157510812A>T	GRCh37
NC_000006.10:g.157552504A>T	NCBI36
NG_032093.1:g.416749A>T
NG_032093.2:g.416749A>T
NG_066624.1:g.418653A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3797A>T	ENSP00000055163.8:p.Gln1266Leu
ENST00000414678.8:c.3866A>T	ENSP00000412835.3:p.Gln1289Leu
ENST00000637015.2:c.4085A>T	ENSP00000489729.2:p.Gln1362Leu
ENST00000346085.10:c.3836A>T	ENSP00000344546.5:p.Gln1279Leu
ENST00000350026.10:c.3548A>T	ENSP00000055163.7:p.Gln1183Leu
ENST00000414678.7:c.2114A>T	ENSP00000412835.2:p.Gln705Leu
ENST00000635849.1:c.1277A>T	ENSP00000490948.1:p.Gln426Leu
ENST00000635957.1:c.911A>T	ENSP00000490385.1:p.Gln304Leu
ENST00000636930.2:c.3956A>T MANE Select	ENSP00000490491.2:p.Gln1319Leu
ENST00000636940.1:n.1953A>T
ENST00000637015.1:c.1324A>T
ENST00000637568.1:c.1238A>T
ENST00000637741.1:n.622A>T
ENST00000637810.1:c.1298A>T	ENSP00000489636.1:p.Gln433Leu
ENST00000637904.1:c.1457A>T	ENSP00000490550.1:p.Gln486Leu
ENST00000647938.1:c.3587A>T	ENSP00000498155.1:p.Gln1196Leu
ENST00000346085.9:c.3587A>T	ENSP00000344546.4:p.Gln1196Leu
ENST00000350026.9:c.3548A>T	ENSP00000055163.7:p.Gln1183Leu
ENST00000414678.6:c.2114A>T	ENSP00000412835.2:p.Gln705Leu
NM_017519.2:c.3548A>T	NP_059989.2:p.Gln1183Leu
NM_020732.3:c.3587A>T	NP_065783.3:p.Gln1196Leu
XM_005267069.3:c.3707A>T	XP_005267126.2:p.Gln1236Leu
XM_011535984.1:c.2786A>T	XP_011534286.1:p.Gln929Leu
XM_011535985.1:c.2606A>T	XP_011534287.1:p.Gln869Leu
XM_011535986.1:c.2366A>T	XP_011534288.1:p.Gln789Leu
XM_011535987.1:c.1985A>T	XP_011534289.1:p.Gln662Leu
XM_011535988.1:c.848A>T	XP_011534290.1:p.Gln283Leu
NM_001346813.1:c.3707A>T	NP_001333742.1:p.Gln1236Leu
NM_001363725.1:c.1457A>T	NP_001350654.1:p.Gln486Leu
XM_011535984.2:c.3917A>T	XP_011534286.2:p.Gln1306Leu
XM_011535988.3:c.848A>T	XP_011534290.1:p.Gln283Leu
XM_017011103.2:c.3818A>T	XP_016866592.1:p.Gln1273Leu
XM_017011104.1:c.3788A>T	XP_016866593.1:p.Gln1263Leu
XM_017011105.2:c.3758A>T	XP_016866594.1:p.Gln1253Leu
XM_017011106.2:c.3629A>T	XP_016866595.1:p.Gln1210Leu
XM_017011107.2:c.3608A>T	XP_016866596.1:p.Gln1203Leu
XR_002956289.1:n.4000A>T
NM_001363725.2:c.1457A>T	NP_001350654.1:p.Gln486Leu
NM_001371656.1:c.3836A>T	NP_001358585.1:p.Gln1279Leu
NM_001374820.1:c.3836A>T	NP_001361749.1:p.Gln1279Leu
NM_001374828.1:c.3956A>T MANE Select	NP_001361757.1:p.Gln1319Leu
NM_017519.3:c.3797A>T	NP_059989.3:p.Gln1266Leu