Canonical Allele Identifier: CA1675542326

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157199076A= , CM000668.2:g.157199076A=	GRCh38
NC_000006.11:g.157520210A= , CM000668.1:g.157520210A=	GRCh37
NC_000006.10:g.157561902A=	NCBI36
NG_032093.1:g.426147A=
NG_032093.2:g.426147A=
NG_066624.1:g.428051A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+169A=	ENSP00000055163.8:n.4320+169A=
ENST00000414678.8:c.4389+169A=	ENSP00000412835.3:n.4389+169A=
ENST00000637015.2:c.4608+169A=	ENSP00000489729.2:n.4608+169A=
ENST00000346085.10:c.4359+169A=	ENSP00000344546.5:n.4359+169A=
ENST00000350026.10:c.4071+169A=	ENSP00000055163.7:n.4071+169A=
ENST00000414678.7:c.2637+169A=	ENSP00000412835.2:n.2637+169A=
ENST00000635849.1:c.1800+169A=	ENSP00000490948.1:n.1800+169A=
ENST00000635957.1:c.1431+169A=	ENSP00000490385.1:n.1431+169A=
ENST00000636227.1:n.2942+169A=
ENST00000636254.1:n.399+169A=
ENST00000636930.2:c.4479+169A= MANE Select	ENSP00000490491.2:n.4479+169A=
ENST00000636940.1:n.2476+169A=
ENST00000637015.1:c.1847+169A=
ENST00000637568.1:c.1761+169A=
ENST00000637741.1:n.1145+169A=
ENST00000637810.1:c.1821+169A=	ENSP00000489636.1:n.1821+169A=
ENST00000637904.1:c.1980+169A=	ENSP00000490550.1:n.1980+169A=
ENST00000647938.1:c.4110+169A=	ENSP00000498155.1:n.4110+169A=
ENST00000346085.9:c.4110+169A=	ENSP00000344546.4:n.4110+169A=
ENST00000350026.9:c.4071+169A=	ENSP00000055163.7:n.4071+169A=
ENST00000414678.6:c.2637+169A=	ENSP00000412835.2:n.2637+169A=
NM_017519.2:c.4071+169A=	NP_059989.2:n.4071+169A=
NM_020732.3:c.4110+169A=	NP_065783.3:n.4110+169A=
XM_005267069.3:c.4230+169A=	XP_005267126.2:n.4230+169A=
XM_011535984.1:c.3309+169A=	XP_011534286.1:n.3309+169A=
XM_011535985.1:c.3129+169A=	XP_011534287.1:n.3129+169A=
XM_011535986.1:c.2889+169A=	XP_011534288.1:n.2889+169A=
XM_011535987.1:c.2508+169A=	XP_011534289.1:n.2508+169A=
XM_011535988.1:c.1371+169A=	XP_011534290.1:n.1371+169A=
NM_001346813.1:c.4230+169A=	NP_001333742.1:n.4230+169A=
NM_001363725.1:c.1980+169A=	NP_001350654.1:n.1980+169A=
XM_011535984.2:c.4440+169A=	XP_011534286.2:n.4440+169A=
XM_011535988.3:c.1371+169A=	XP_011534290.1:n.1371+169A=
XM_017011103.2:c.4341+169A=	XP_016866592.1:n.4341+169A=
XM_017011104.1:c.4311+169A=	XP_016866593.1:n.4311+169A=
XM_017011105.2:c.4281+169A=	XP_016866594.1:n.4281+169A=
XM_017011106.2:c.4152+169A=	XP_016866595.1:n.4152+169A=
XM_017011107.2:c.4131+169A=	XP_016866596.1:n.4131+169A=
XR_002956289.1:n.4427-1629A=
NM_001363725.2:c.1980+169A=	NP_001350654.1:n.1980+169A=
NM_001371656.1:c.4359+169A=	NP_001358585.1:n.4359+169A=
NM_001374820.1:c.4359+169A=	NP_001361749.1:n.4359+169A=
NM_001374828.1:c.4479+169A= MANE Select	NP_001361757.1:n.4479+169A=
NM_017519.3:c.4320+169A=	NP_059989.3:n.4320+169A=