Canonical Allele Identifier: CA205671

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156935534A>T , CM000668.2:g.156935534A>T	GRCh38
NC_000006.11:g.157256668A>T , CM000668.1:g.157256668A>T	GRCh37
NC_000006.10:g.157298360A>T	NCBI36
NG_032093.1:g.162605A>T
NG_032093.2:g.162605A>T
NG_066624.1:g.164509A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.2205A>T MANE Select	NP_001361757.1:p.Glu735Asp
ENST00000636930.2:c.2205A>T MANE Select	ENSP00000490491.2:p.Glu735Asp
NM_001346813.1:c.1956A>T	NP_001333742.1:p.Glu652Asp
NM_001371656.1:c.2244A>T	NP_001358585.1:p.Glu748Asp
NM_001374820.1:c.2244A>T	NP_001361749.1:p.Glu748Asp
NM_017519.2:c.1956A>T	NP_059989.2:p.Glu652Asp
NM_017519.3:c.2205A>T	NP_059989.3:p.Glu735Asp
NM_020732.3:c.1995A>T	NP_065783.3:p.Glu665Asp
ENST00000319584.10:c.222A>T	ENSP00000313006.6:p.Glu74Asp
ENST00000319584.11:c.219A>T	ENSP00000313006.7:p.Glu73Asp
ENST00000346085.10:c.2244A>T	ENSP00000344546.5:p.Glu748Asp
ENST00000346085.9:c.1995A>T	ENSP00000344546.4:p.Glu665Asp
ENST00000350026.10:c.1956A>T	ENSP00000055163.7:p.Glu652Asp
ENST00000350026.11:c.2205A>T	ENSP00000055163.8:p.Glu735Asp
ENST00000350026.9:c.1956A>T	ENSP00000055163.7:p.Glu652Asp
ENST00000414678.6:c.453A>T	ENSP00000412835.2:p.Glu151Asp
ENST00000414678.7:c.453A>T	ENSP00000412835.2:p.Glu151Asp
ENST00000414678.8:c.2205A>T	ENSP00000412835.3:p.Glu735Asp
ENST00000452544.1:n.64A>T
ENST00000452544.2:n.64A>T
ENST00000636748.1:c.486A>T	ENSP00000489917.1:p.Glu162Asp
ENST00000637015.2:c.2205A>T	ENSP00000489729.2:p.Glu735Asp
ENST00000637532.1:c.231A>T	ENSP00000490420.1:p.Glu77Asp
ENST00000638000.1:c.422A>T
ENST00000647938.1:c.1995A>T	ENSP00000498155.1:p.Glu665Asp
ENST00000674190.1:n.912A>T
ENST00000674298.1:c.1945A>T
XM_005267069.3:c.1956A>T	XP_005267126.2:p.Glu652Asp
XM_011535984.1:c.864A>T	XP_011534286.1:p.Glu288Asp
XM_011535984.2:c.1995A>T	XP_011534286.2:p.Glu665Asp
XM_011535985.1:c.864A>T	XP_011534287.1:p.Glu288Asp
XM_011535986.1:c.444A>T	XP_011534288.1:p.Glu148Asp
XM_017011103.2:c.1995A>T	XP_016866592.1:p.Glu665Asp
XM_017011104.1:c.1995A>T	XP_016866593.1:p.Glu665Asp
XM_017011105.2:c.1995A>T	XP_016866594.1:p.Glu665Asp
XM_017011106.2:c.1995A>T	XP_016866595.1:p.Glu665Asp
XM_017011107.2:c.1995A>T	XP_016866596.1:p.Glu665Asp
XR_002956289.1:n.2078A>T