Canonical Allele Identifier: CA1675538408

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190110G= , CM000668.2:g.157190110G=	GRCh38
NC_000006.11:g.157511244G= , CM000668.1:g.157511244G=	GRCh37
NC_000006.10:g.157552936G=	NCBI36
NG_032093.1:g.417181G=
NG_032093.2:g.417181G=
NG_066624.1:g.419085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3972G=	ENSP00000055163.8:p.Met1324=
ENST00000414678.8:c.4041G=	ENSP00000412835.3:p.Met1347=
ENST00000637015.2:c.4260G=	ENSP00000489729.2:p.Met1420=
ENST00000346085.10:c.4011G=	ENSP00000344546.5:p.Met1337=
ENST00000350026.10:c.3723G=	ENSP00000055163.7:p.Met1241=
ENST00000414678.7:c.2289G=	ENSP00000412835.2:p.Met763=
ENST00000635849.1:c.1452G=	ENSP00000490948.1:p.Met484=
ENST00000635957.1:c.1083G=	ENSP00000490385.1:p.Met361=
ENST00000636930.2:c.4131G= MANE Select	ENSP00000490491.2:p.Met1377=
ENST00000636940.1:n.2128G=
ENST00000637015.1:c.1499G=
ENST00000637568.1:c.1413G=
ENST00000637741.1:n.797G=
ENST00000637810.1:c.1473G=	ENSP00000489636.1:p.Met491=
ENST00000637904.1:c.1632G=	ENSP00000490550.1:p.Met544=
ENST00000647938.1:c.3762G=	ENSP00000498155.1:p.Met1254=
ENST00000346085.9:c.3762G=	ENSP00000344546.4:p.Met1254=
ENST00000350026.9:c.3723G=	ENSP00000055163.7:p.Met1241=
ENST00000414678.6:c.2289G=	ENSP00000412835.2:p.Met763=
NM_017519.2:c.3723G=	NP_059989.2:p.Met1241=
NM_020732.3:c.3762G=	NP_065783.3:p.Met1254=
XM_005267069.3:c.3882G=	XP_005267126.2:p.Met1294=
XM_011535984.1:c.2961G=	XP_011534286.1:p.Met987=
XM_011535985.1:c.2781G=	XP_011534287.1:p.Met927=
XM_011535986.1:c.2541G=	XP_011534288.1:p.Met847=
XM_011535987.1:c.2160G=	XP_011534289.1:p.Met720=
XM_011535988.1:c.1023G=	XP_011534290.1:p.Met341=
NM_001346813.1:c.3882G=	NP_001333742.1:p.Met1294=
NM_001363725.1:c.1632G=	NP_001350654.1:p.Met544=
XM_011535984.2:c.4092G=	XP_011534286.2:p.Met1364=
XM_011535988.3:c.1023G=	XP_011534290.1:p.Met341=
XM_017011103.2:c.3993G=	XP_016866592.1:p.Met1331=
XM_017011104.1:c.3963G=	XP_016866593.1:p.Met1321=
XM_017011105.2:c.3933G=	XP_016866594.1:p.Met1311=
XM_017011106.2:c.3804G=	XP_016866595.1:p.Met1268=
XM_017011107.2:c.3783G=	XP_016866596.1:p.Met1261=
XR_002956289.1:n.4175G=
NM_001363725.2:c.1632G=	NP_001350654.1:p.Met544=
NM_001371656.1:c.4011G=	NP_001358585.1:p.Met1337=
NM_001374820.1:c.4011G=	NP_001361749.1:p.Met1337=
NM_001374828.1:c.4131G= MANE Select	NP_001361757.1:p.Met1377=
NM_017519.3:c.3972G=	NP_059989.3:p.Met1324=