Canonical Allele Identifier: CA1675542238

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198867C= , CM000668.2:g.157198867C=	GRCh38
NC_000006.11:g.157520001C= , CM000668.1:g.157520001C=	GRCh37
NC_000006.10:g.157561693C=	NCBI36
NG_032093.1:g.425938C=
NG_032093.2:g.425938C=
NG_066624.1:g.427842C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4280C=	ENSP00000055163.8:p.Pro1427=
ENST00000414678.8:c.4349C=	ENSP00000412835.3:p.Pro1450=
ENST00000637015.2:c.4568C=	ENSP00000489729.2:p.Pro1523=
ENST00000346085.10:c.4319C=	ENSP00000344546.5:p.Pro1440=
ENST00000350026.10:c.4031C=	ENSP00000055163.7:p.Pro1344=
ENST00000414678.7:c.2597C=	ENSP00000412835.2:p.Pro866=
ENST00000635849.1:c.1760C=	ENSP00000490948.1:p.Pro587=
ENST00000635957.1:c.1391C=	ENSP00000490385.1:p.Pro464=
ENST00000636227.1:n.2902C=
ENST00000636254.1:n.359C=
ENST00000636930.2:c.4439C= MANE Select	ENSP00000490491.2:p.Pro1480=
ENST00000636940.1:n.2436C=
ENST00000637015.1:c.1807C=
ENST00000637568.1:c.1721C=
ENST00000637741.1:n.1105C=
ENST00000637810.1:c.1781C=	ENSP00000489636.1:p.Pro594=
ENST00000637904.1:c.1940C=	ENSP00000490550.1:p.Pro647=
ENST00000647938.1:c.4070C=	ENSP00000498155.1:p.Pro1357=
ENST00000346085.9:c.4070C=	ENSP00000344546.4:p.Pro1357=
ENST00000350026.9:c.4031C=	ENSP00000055163.7:p.Pro1344=
ENST00000414678.6:c.2597C=	ENSP00000412835.2:p.Pro866=
NM_017519.2:c.4031C=	NP_059989.2:p.Pro1344=
NM_020732.3:c.4070C=	NP_065783.3:p.Pro1357=
XM_005267069.3:c.4190C=	XP_005267126.2:p.Pro1397=
XM_011535984.1:c.3269C=	XP_011534286.1:p.Pro1090=
XM_011535985.1:c.3089C=	XP_011534287.1:p.Pro1030=
XM_011535986.1:c.2849C=	XP_011534288.1:p.Pro950=
XM_011535987.1:c.2468C=	XP_011534289.1:p.Pro823=
XM_011535988.1:c.1331C=	XP_011534290.1:p.Pro444=
NM_001346813.1:c.4190C=	NP_001333742.1:p.Pro1397=
NM_001363725.1:c.1940C=	NP_001350654.1:p.Pro647=
XM_011535984.2:c.4400C=	XP_011534286.2:p.Pro1467=
XM_011535988.3:c.1331C=	XP_011534290.1:p.Pro444=
XM_017011103.2:c.4301C=	XP_016866592.1:p.Pro1434=
XM_017011104.1:c.4271C=	XP_016866593.1:p.Pro1424=
XM_017011105.2:c.4241C=	XP_016866594.1:p.Pro1414=
XM_017011106.2:c.4112C=	XP_016866595.1:p.Pro1371=
XM_017011107.2:c.4091C=	XP_016866596.1:p.Pro1364=
XR_002956289.1:n.4427-1838C=
NM_001363725.2:c.1940C=	NP_001350654.1:p.Pro647=
NM_001371656.1:c.4319C=	NP_001358585.1:p.Pro1440=
NM_001374820.1:c.4319C=	NP_001361749.1:p.Pro1440=
NM_001374828.1:c.4439C= MANE Select	NP_001361757.1:p.Pro1480=
NM_017519.3:c.4280C=	NP_059989.3:p.Pro1427=