Canonical Allele Identifier: CA1675538269

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189758A= , CM000668.2:g.157189758A=	GRCh38
NC_000006.11:g.157510892A= , CM000668.1:g.157510892A=	GRCh37
NC_000006.10:g.157552584A=	NCBI36
NG_032093.1:g.416829A=
NG_032093.2:g.416829A=
NG_066624.1:g.418733A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3877A=	ENSP00000055163.8:p.Met1293=
ENST00000414678.8:c.3946A=	ENSP00000412835.3:p.Met1316=
ENST00000637015.2:c.4165A=	ENSP00000489729.2:p.Met1389=
ENST00000346085.10:c.3916A=	ENSP00000344546.5:p.Met1306=
ENST00000350026.10:c.3628A=	ENSP00000055163.7:p.Met1210=
ENST00000414678.7:c.2194A=	ENSP00000412835.2:p.Met732=
ENST00000635849.1:c.1357A=	ENSP00000490948.1:p.Met453=
ENST00000635957.1:c.991A=	ENSP00000490385.1:p.Met331=
ENST00000636930.2:c.4036A= MANE Select	ENSP00000490491.2:p.Met1346=
ENST00000636940.1:n.2033A=
ENST00000637015.1:c.1404A=
ENST00000637568.1:c.1318A=
ENST00000637741.1:n.702A=
ENST00000637810.1:c.1378A=	ENSP00000489636.1:p.Met460=
ENST00000637904.1:c.1537A=	ENSP00000490550.1:p.Met513=
ENST00000647938.1:c.3667A=	ENSP00000498155.1:p.Met1223=
ENST00000346085.9:c.3667A=	ENSP00000344546.4:p.Met1223=
ENST00000350026.9:c.3628A=	ENSP00000055163.7:p.Met1210=
ENST00000414678.6:c.2194A=	ENSP00000412835.2:p.Met732=
NM_017519.2:c.3628A=	NP_059989.2:p.Met1210=
NM_020732.3:c.3667A=	NP_065783.3:p.Met1223=
XM_005267069.3:c.3787A=	XP_005267126.2:p.Met1263=
XM_011535984.1:c.2866A=	XP_011534286.1:p.Met956=
XM_011535985.1:c.2686A=	XP_011534287.1:p.Met896=
XM_011535986.1:c.2446A=	XP_011534288.1:p.Met816=
XM_011535987.1:c.2065A=	XP_011534289.1:p.Met689=
XM_011535988.1:c.928A=	XP_011534290.1:p.Met310=
NM_001346813.1:c.3787A=	NP_001333742.1:p.Met1263=
NM_001363725.1:c.1537A=	NP_001350654.1:p.Met513=
XM_011535984.2:c.3997A=	XP_011534286.2:p.Met1333=
XM_011535988.3:c.928A=	XP_011534290.1:p.Met310=
XM_017011103.2:c.3898A=	XP_016866592.1:p.Met1300=
XM_017011104.1:c.3868A=	XP_016866593.1:p.Met1290=
XM_017011105.2:c.3838A=	XP_016866594.1:p.Met1280=
XM_017011106.2:c.3709A=	XP_016866595.1:p.Met1237=
XM_017011107.2:c.3688A=	XP_016866596.1:p.Met1230=
XR_002956289.1:n.4080A=
NM_001363725.2:c.1537A=	NP_001350654.1:p.Met513=
NM_001371656.1:c.3916A=	NP_001358585.1:p.Met1306=
NM_001374820.1:c.3916A=	NP_001361749.1:p.Met1306=
NM_001374828.1:c.4036A= MANE Select	NP_001361757.1:p.Met1346=
NM_017519.3:c.3877A=	NP_059989.3:p.Met1293=