Canonical Allele Identifier: CA1675517010

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148765G= , CM000668.2:g.157148765G=	GRCh38
NC_000006.11:g.157469899G= , CM000668.1:g.157469899G=	GRCh37
NC_000006.10:g.157511591G=	NCBI36
NG_032093.1:g.375836G=
NG_032093.2:g.375836G=
NG_066624.1:g.377740G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2903G=	ENSP00000055163.8:p.Arg968=
ENST00000414678.8:c.2813G=	ENSP00000412835.3:p.Arg938=
ENST00000637015.2:c.2903G=	ENSP00000489729.2:p.Arg968=
ENST00000319584.11:c.917G=	ENSP00000313006.7:p.Arg306=
ENST00000346085.10:c.2942G=	ENSP00000344546.5:p.Arg981=
ENST00000350026.10:c.2654G=	ENSP00000055163.7:p.Arg885=
ENST00000414678.7:c.1061G=	ENSP00000412835.2:p.Arg354=
ENST00000452544.2:n.804G=
ENST00000635849.1:c.224G=	ENSP00000490948.1:p.Arg75=
ENST00000636426.1:n.37G=
ENST00000636930.2:c.2903G= MANE Select	ENSP00000490491.2:p.Arg968=
ENST00000637015.1:c.142G=
ENST00000637810.1:c.404G=	ENSP00000489636.1:p.Arg135=
ENST00000637904.1:c.404G=	ENSP00000490550.1:p.Arg135=
ENST00000647938.1:c.2693G=	ENSP00000498155.1:p.Arg898=
ENST00000674190.1:n.1652G=
ENST00000319584.10:c.920G=	ENSP00000313006.6:p.Arg307=
ENST00000346085.9:c.2693G=	ENSP00000344546.4:p.Arg898=
ENST00000350026.9:c.2654G=	ENSP00000055163.7:p.Arg885=
ENST00000414678.6:c.1061G=	ENSP00000412835.2:p.Arg354=
ENST00000452544.1:n.750G=
NM_017519.2:c.2654G=	NP_059989.2:p.Arg885=
NM_020732.3:c.2693G=	NP_065783.3:p.Arg898=
XM_005267069.3:c.2654G=	XP_005267126.2:p.Arg885=
XM_011535984.1:c.1604G=	XP_011534286.1:p.Arg535=
XM_011535985.1:c.1424G=	XP_011534287.1:p.Arg475=
XM_011535986.1:c.1184G=	XP_011534288.1:p.Arg395=
XM_011535987.1:c.803G=	XP_011534289.1:p.Arg268=
XM_011535988.1:c.-20+15558G=	XP_011534290.1:n.-20+15558G=
NM_001346813.1:c.2654G=	NP_001333742.1:p.Arg885=
NM_001363725.1:c.404G=	NP_001350654.1:p.Arg135=
XM_011535984.2:c.2735G=	XP_011534286.2:p.Arg912=
XM_011535988.3:c.-20+15558G=	XP_011534290.1:n.-20+15558G=
XM_017011103.2:c.2735G=	XP_016866592.1:p.Arg912=
XM_017011104.1:c.2735G=	XP_016866593.1:p.Arg912=
XM_017011105.2:c.2735G=	XP_016866594.1:p.Arg912=
XM_017011106.2:c.2735G=	XP_016866595.1:p.Arg912=
XM_017011107.2:c.2555G=	XP_016866596.1:p.Arg852=
XR_002956289.1:n.2818G=
NM_001363725.2:c.404G=	NP_001350654.1:p.Arg135=
NM_001371656.1:c.2942G=	NP_001358585.1:p.Arg981=
NM_001374820.1:c.2942G=	NP_001361749.1:p.Arg981=
NM_001374828.1:c.2903G= MANE Select	NP_001361757.1:p.Arg968=
NM_017519.3:c.2903G=	NP_059989.3:p.Arg968=