Canonical Allele Identifier: CA1675517060

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148883T= , CM000668.2:g.157148883T=	GRCh38
NC_000006.11:g.157470017T= , CM000668.1:g.157470017T=	GRCh37
NC_000006.10:g.157511709T=	NCBI36
NG_032093.1:g.375954T=
NG_032093.2:g.375954T=
NG_066624.1:g.377858T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3021T=	ENSP00000055163.8:p.Thr1007=
ENST00000414678.8:c.2931T=	ENSP00000412835.3:p.Thr977=
ENST00000637015.2:c.3021T=	ENSP00000489729.2:p.Thr1007=
ENST00000319584.11:c.1035T=	ENSP00000313006.7:p.Thr345=
ENST00000346085.10:c.3060T=	ENSP00000344546.5:p.Thr1020=
ENST00000350026.10:c.2772T=	ENSP00000055163.7:p.Thr924=
ENST00000414678.7:c.1179T=	ENSP00000412835.2:p.Thr393=
ENST00000452544.2:n.922T=
ENST00000635849.1:c.342T=	ENSP00000490948.1:p.Thr114=
ENST00000636426.1:n.155T=
ENST00000636930.2:c.3021T= MANE Select	ENSP00000490491.2:p.Thr1007=
ENST00000637015.1:c.260T=
ENST00000637568.1:c.64T=
ENST00000637810.1:c.522T=	ENSP00000489636.1:p.Thr174=
ENST00000637904.1:c.522T=	ENSP00000490550.1:p.Thr174=
ENST00000647938.1:c.2811T=	ENSP00000498155.1:p.Thr937=
ENST00000674190.1:n.1770T=
ENST00000319584.10:c.1038T=	ENSP00000313006.6:p.Thr346=
ENST00000346085.9:c.2811T=	ENSP00000344546.4:p.Thr937=
ENST00000350026.9:c.2772T=	ENSP00000055163.7:p.Thr924=
ENST00000414678.6:c.1179T=	ENSP00000412835.2:p.Thr393=
ENST00000452544.1:n.868T=
ENST00000478761.3:c.94T=
NM_017519.2:c.2772T=	NP_059989.2:p.Thr924=
NM_020732.3:c.2811T=	NP_065783.3:p.Thr937=
XM_005267069.3:c.2772T=	XP_005267126.2:p.Thr924=
XM_011535984.1:c.1722T=	XP_011534286.1:p.Thr574=
XM_011535985.1:c.1542T=	XP_011534287.1:p.Thr514=
XM_011535986.1:c.1302T=	XP_011534288.1:p.Thr434=
XM_011535987.1:c.921T=	XP_011534289.1:p.Thr307=
XM_011535988.1:c.-20+15676T=	XP_011534290.1:n.-20+15676T=
NM_001346813.1:c.2772T=	NP_001333742.1:p.Thr924=
NM_001363725.1:c.522T=	NP_001350654.1:p.Thr174=
XM_011535984.2:c.2853T=	XP_011534286.2:p.Thr951=
XM_011535988.3:c.-20+15676T=	XP_011534290.1:n.-20+15676T=
XM_017011103.2:c.2853T=	XP_016866592.1:p.Thr951=
XM_017011104.1:c.2853T=	XP_016866593.1:p.Thr951=
XM_017011105.2:c.2853T=	XP_016866594.1:p.Thr951=
XM_017011106.2:c.2853T=	XP_016866595.1:p.Thr951=
XM_017011107.2:c.2673T=	XP_016866596.1:p.Thr891=
XR_002956289.1:n.2936T=
NM_001363725.2:c.522T=	NP_001350654.1:p.Thr174=
NM_001371656.1:c.3060T=	NP_001358585.1:p.Thr1020=
NM_001374820.1:c.3060T=	NP_001361749.1:p.Thr1020=
NM_001374828.1:c.3021T= MANE Select	NP_001361757.1:p.Thr1007=
NM_017519.3:c.3021T=	NP_059989.3:p.Thr1007=