Canonical Allele Identifier: CA1675534233

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181041A= , CM000668.2:g.157181041A=	GRCh38
NC_000006.11:g.157502175A= , CM000668.1:g.157502175A=	GRCh37
NC_000006.10:g.157543867A=	NCBI36
NG_032093.1:g.408112A=
NG_032093.2:g.408112A=
NG_066624.1:g.410016A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3418A=	ENSP00000055163.8:p.Lys1140=
ENST00000414678.8:c.3487A=	ENSP00000412835.3:p.Lys1163=
ENST00000637015.2:c.3706A=	ENSP00000489729.2:p.Lys1236=
ENST00000319584.11:c.1591A=	ENSP00000313006.7:p.Lys531=
ENST00000346085.10:c.3457A=	ENSP00000344546.5:p.Lys1153=
ENST00000350026.10:c.3169A=	ENSP00000055163.7:p.Lys1057=
ENST00000414678.7:c.1735A=	ENSP00000412835.2:p.Lys579=
ENST00000635849.1:c.898A=	ENSP00000490948.1:p.Lys300=
ENST00000635957.1:c.532A=	ENSP00000490385.1:p.Lys178=
ENST00000636930.2:c.3577A= MANE Select	ENSP00000490491.2:p.Lys1193=
ENST00000636940.1:n.1574A=
ENST00000637015.1:c.945A=
ENST00000637568.1:c.859A=
ENST00000637741.1:n.243A=
ENST00000637810.1:c.919A=	ENSP00000489636.1:p.Lys307=
ENST00000637904.1:c.1078A=	ENSP00000490550.1:p.Lys360=
ENST00000647938.1:c.3208A=	ENSP00000498155.1:p.Lys1070=
ENST00000319584.10:c.1594A=	ENSP00000313006.6:p.Lys532=
ENST00000346085.9:c.3208A=	ENSP00000344546.4:p.Lys1070=
ENST00000350026.9:c.3169A=	ENSP00000055163.7:p.Lys1057=
ENST00000400790.3:c.370A=	ENSP00000383596.3:p.Lys124=
ENST00000414678.6:c.1735A=	ENSP00000412835.2:p.Lys579=
ENST00000478761.3:c.779A=
NM_017519.2:c.3169A=	NP_059989.2:p.Lys1057=
NM_020732.3:c.3208A=	NP_065783.3:p.Lys1070=
XM_005267069.3:c.3328A=	XP_005267126.2:p.Lys1110=
XM_011535984.1:c.2407A=	XP_011534286.1:p.Lys803=
XM_011535985.1:c.2227A=	XP_011534287.1:p.Lys743=
XM_011535986.1:c.1987A=	XP_011534288.1:p.Lys663=
XM_011535987.1:c.1606A=	XP_011534289.1:p.Lys536=
XM_011535988.1:c.469A=	XP_011534290.1:p.Lys157=
NM_001346813.1:c.3328A=	NP_001333742.1:p.Lys1110=
NM_001363725.1:c.1078A=	NP_001350654.1:p.Lys360=
XM_011535984.2:c.3538A=	XP_011534286.2:p.Lys1180=
XM_011535988.3:c.469A=	XP_011534290.1:p.Lys157=
XM_017011103.2:c.3439A=	XP_016866592.1:p.Lys1147=
XM_017011104.1:c.3409A=	XP_016866593.1:p.Lys1137=
XM_017011105.2:c.3379A=	XP_016866594.1:p.Lys1127=
XM_017011106.2:c.3250A=	XP_016866595.1:p.Lys1084=
XM_017011107.2:c.3229A=	XP_016866596.1:p.Lys1077=
XR_002956289.1:n.3621A=
NM_001363725.2:c.1078A=	NP_001350654.1:p.Lys360=
NM_001371656.1:c.3457A=	NP_001358585.1:p.Lys1153=
NM_001374820.1:c.3457A=	NP_001361749.1:p.Lys1153=
NM_001374828.1:c.3577A= MANE Select	NP_001361757.1:p.Lys1193=
NM_017519.3:c.3418A=	NP_059989.3:p.Lys1140=