Canonical Allele Identifier: CA1675542226

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198842C= , CM000668.2:g.157198842C=	GRCh38
NC_000006.11:g.157519976C= , CM000668.1:g.157519976C=	GRCh37
NC_000006.10:g.157561668C=	NCBI36
NG_032093.1:g.425913C=
NG_032093.2:g.425913C=
NG_066624.1:g.427817C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4255C=	ENSP00000055163.8:p.Gln1419=
ENST00000414678.8:c.4324C=	ENSP00000412835.3:p.Gln1442=
ENST00000637015.2:c.4543C=	ENSP00000489729.2:p.Gln1515=
ENST00000346085.10:c.4294C=	ENSP00000344546.5:p.Gln1432=
ENST00000350026.10:c.4006C=	ENSP00000055163.7:p.Gln1336=
ENST00000414678.7:c.2572C=	ENSP00000412835.2:p.Gln858=
ENST00000635849.1:c.1735C=	ENSP00000490948.1:p.Gln579=
ENST00000635957.1:c.1366C=	ENSP00000490385.1:p.Gln456=
ENST00000636227.1:n.2877C=
ENST00000636254.1:n.334C=
ENST00000636930.2:c.4414C= MANE Select	ENSP00000490491.2:p.Gln1472=
ENST00000636940.1:n.2411C=
ENST00000637015.1:c.1782C=
ENST00000637568.1:c.1696C=
ENST00000637741.1:n.1080C=
ENST00000637810.1:c.1756C=	ENSP00000489636.1:p.Gln586=
ENST00000637904.1:c.1915C=	ENSP00000490550.1:p.Gln639=
ENST00000647938.1:c.4045C=	ENSP00000498155.1:p.Gln1349=
ENST00000346085.9:c.4045C=	ENSP00000344546.4:p.Gln1349=
ENST00000350026.9:c.4006C=	ENSP00000055163.7:p.Gln1336=
ENST00000414678.6:c.2572C=	ENSP00000412835.2:p.Gln858=
NM_017519.2:c.4006C=	NP_059989.2:p.Gln1336=
NM_020732.3:c.4045C=	NP_065783.3:p.Gln1349=
XM_005267069.3:c.4165C=	XP_005267126.2:p.Gln1389=
XM_011535984.1:c.3244C=	XP_011534286.1:p.Gln1082=
XM_011535985.1:c.3064C=	XP_011534287.1:p.Gln1022=
XM_011535986.1:c.2824C=	XP_011534288.1:p.Gln942=
XM_011535987.1:c.2443C=	XP_011534289.1:p.Gln815=
XM_011535988.1:c.1306C=	XP_011534290.1:p.Gln436=
NM_001346813.1:c.4165C=	NP_001333742.1:p.Gln1389=
NM_001363725.1:c.1915C=	NP_001350654.1:p.Gln639=
XM_011535984.2:c.4375C=	XP_011534286.2:p.Gln1459=
XM_011535988.3:c.1306C=	XP_011534290.1:p.Gln436=
XM_017011103.2:c.4276C=	XP_016866592.1:p.Gln1426=
XM_017011104.1:c.4246C=	XP_016866593.1:p.Gln1416=
XM_017011105.2:c.4216C=	XP_016866594.1:p.Gln1406=
XM_017011106.2:c.4087C=	XP_016866595.1:p.Gln1363=
XM_017011107.2:c.4066C=	XP_016866596.1:p.Gln1356=
XR_002956289.1:n.4427-1863C=
NM_001363725.2:c.1915C=	NP_001350654.1:p.Gln639=
NM_001371656.1:c.4294C=	NP_001358585.1:p.Gln1432=
NM_001374820.1:c.4294C=	NP_001361749.1:p.Gln1432=
NM_001374828.1:c.4414C= MANE Select	NP_001361757.1:p.Gln1472=
NM_017519.3:c.4255C=	NP_059989.3:p.Gln1419=