Canonical Allele Identifier: CA1675523004

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201118T= , CM000668.2:g.157201118T=	GRCh38
NC_000006.11:g.157522252T= , CM000668.1:g.157522252T=	GRCh37
NC_000006.10:g.157563944T=	NCBI36
NG_032093.1:g.428189T=
NG_032093.2:g.428189T=
NG_066624.1:g.430093T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4734T=	ENSP00000055163.8:p.His1578=
ENST00000414678.8:c.4803T=	ENSP00000412835.3:p.His1601=
ENST00000637015.2:c.5022T=	ENSP00000489729.2:p.His1674=
ENST00000346085.10:c.4773T=	ENSP00000344546.5:p.His1591=
ENST00000350026.10:c.4485T=	ENSP00000055163.7:p.His1495=
ENST00000414678.7:c.3051T=	ENSP00000412835.2:p.His1017=
ENST00000635849.1:c.2214T=	ENSP00000490948.1:p.His738=
ENST00000635957.1:c.1845T=	ENSP00000490385.1:p.His615=
ENST00000636227.1:n.3356T=
ENST00000636254.1:n.813T=
ENST00000636930.2:c.4893T= MANE Select	ENSP00000490491.2:p.His1631=
ENST00000636940.1:n.2890T=
ENST00000637015.1:c.2261T=
ENST00000637568.1:c.2175T=
ENST00000637741.1:n.1559T=
ENST00000637810.1:c.2235T=	ENSP00000489636.1:p.His745=
ENST00000637904.1:c.2394T=	ENSP00000490550.1:p.His798=
ENST00000647938.1:c.4524T=	ENSP00000498155.1:p.His1508=
ENST00000346085.9:c.4524T=	ENSP00000344546.4:p.His1508=
ENST00000350026.9:c.4485T=	ENSP00000055163.7:p.His1495=
ENST00000414678.6:c.3051T=	ENSP00000412835.2:p.His1017=
NM_017519.2:c.4485T=	NP_059989.2:p.His1495=
NM_020732.3:c.4524T=	NP_065783.3:p.His1508=
XM_005267069.3:c.4644T=	XP_005267126.2:p.His1548=
XM_011535984.1:c.3723T=	XP_011534286.1:p.His1241=
XM_011535985.1:c.3543T=	XP_011534287.1:p.His1181=
XM_011535986.1:c.3303T=	XP_011534288.1:p.His1101=
XM_011535987.1:c.2922T=	XP_011534289.1:p.His974=
XM_011535988.1:c.1785T=	XP_011534290.1:p.His595=
NM_001346813.1:c.4644T=	NP_001333742.1:p.His1548=
NM_001363725.1:c.2394T=	NP_001350654.1:p.His798=
XM_011535984.2:c.4854T=	XP_011534286.2:p.His1618=
XM_011535988.3:c.1785T=	XP_011534290.1:p.His595=
XM_017011103.2:c.4755T=	XP_016866592.1:p.His1585=
XM_017011104.1:c.4725T=	XP_016866593.1:p.His1575=
XM_017011105.2:c.4695T=	XP_016866594.1:p.His1565=
XM_017011106.2:c.4566T=	XP_016866595.1:p.His1522=
XM_017011107.2:c.4545T=	XP_016866596.1:p.His1515=
XR_002956289.1:n.4840T=
NM_001363725.2:c.2394T=	NP_001350654.1:p.His798=
NM_001371656.1:c.4773T=	NP_001358585.1:p.His1591=
NM_001374820.1:c.4773T=	NP_001361749.1:p.His1591=
NM_001374828.1:c.4893T= MANE Select	NP_001361757.1:p.His1631=
NM_017519.3:c.4734T=	NP_059989.3:p.His1578=