Canonical Allele Identifier: CA1675516996

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148732C= , CM000668.2:g.157148732C=	GRCh38
NC_000006.11:g.157469866C= , CM000668.1:g.157469866C=	GRCh37
NC_000006.10:g.157511558C=	NCBI36
NG_032093.1:g.375803C=
NG_032093.2:g.375803C=
NG_066624.1:g.377707C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2870C=	ENSP00000055163.8:p.Pro957=
ENST00000414678.8:c.2780C=	ENSP00000412835.3:p.Pro927=
ENST00000637015.2:c.2870C=	ENSP00000489729.2:p.Pro957=
ENST00000319584.11:c.884C=	ENSP00000313006.7:p.Pro295=
ENST00000346085.10:c.2909C=	ENSP00000344546.5:p.Pro970=
ENST00000350026.10:c.2621C=	ENSP00000055163.7:p.Pro874=
ENST00000414678.7:c.1028C=	ENSP00000412835.2:p.Pro343=
ENST00000452544.2:n.771C=
ENST00000635849.1:c.191C=	ENSP00000490948.1:p.Pro64=
ENST00000636426.1:n.4C=
ENST00000636930.2:c.2870C= MANE Select	ENSP00000490491.2:p.Pro957=
ENST00000637015.1:c.109C=
ENST00000637810.1:c.371C=	ENSP00000489636.1:p.Pro124=
ENST00000637904.1:c.371C=	ENSP00000490550.1:p.Pro124=
ENST00000647938.1:c.2660C=	ENSP00000498155.1:p.Pro887=
ENST00000674190.1:n.1619C=
ENST00000319584.10:c.887C=	ENSP00000313006.6:p.Pro296=
ENST00000346085.9:c.2660C=	ENSP00000344546.4:p.Pro887=
ENST00000350026.9:c.2621C=	ENSP00000055163.7:p.Pro874=
ENST00000414678.6:c.1028C=	ENSP00000412835.2:p.Pro343=
ENST00000452544.1:n.717C=
NM_017519.2:c.2621C=	NP_059989.2:p.Pro874=
NM_020732.3:c.2660C=	NP_065783.3:p.Pro887=
XM_005267069.3:c.2621C=	XP_005267126.2:p.Pro874=
XM_011535984.1:c.1571C=	XP_011534286.1:p.Pro524=
XM_011535985.1:c.1391C=	XP_011534287.1:p.Pro464=
XM_011535986.1:c.1151C=	XP_011534288.1:p.Pro384=
XM_011535987.1:c.770C=	XP_011534289.1:p.Pro257=
XM_011535988.1:c.-20+15525C=	XP_011534290.1:n.-20+15525C=
NM_001346813.1:c.2621C=	NP_001333742.1:p.Pro874=
NM_001363725.1:c.371C=	NP_001350654.1:p.Pro124=
XM_011535984.2:c.2702C=	XP_011534286.2:p.Pro901=
XM_011535988.3:c.-20+15525C=	XP_011534290.1:n.-20+15525C=
XM_017011103.2:c.2702C=	XP_016866592.1:p.Pro901=
XM_017011104.1:c.2702C=	XP_016866593.1:p.Pro901=
XM_017011105.2:c.2702C=	XP_016866594.1:p.Pro901=
XM_017011106.2:c.2702C=	XP_016866595.1:p.Pro901=
XM_017011107.2:c.2522C=	XP_016866596.1:p.Pro841=
XR_002956289.1:n.2785C=
NM_001363725.2:c.371C=	NP_001350654.1:p.Pro124=
NM_001371656.1:c.2909C=	NP_001358585.1:p.Pro970=
NM_001374820.1:c.2909C=	NP_001361749.1:p.Pro970=
NM_001374828.1:c.2870C= MANE Select	NP_001361757.1:p.Pro957=
NM_017519.3:c.2870C=	NP_059989.3:p.Pro957=