Canonical Allele Identifier: CA366247152

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206698G>T , CM000668.2:g.157206698G>T	GRCh38
NC_000006.11:g.157527832G>T , CM000668.1:g.157527832G>T	GRCh37
NC_000006.10:g.157569524G>T	NCBI36
NG_032093.1:g.433769G>T
NG_032093.2:g.433769G>T
NG_066624.1:g.435673G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5767G>T	ENSP00000055163.8:p.Ala1923Ser
ENST00000414678.8:c.5836G>T	ENSP00000412835.3:p.Ala1946Ser
ENST00000637015.2:c.6055G>T	ENSP00000489729.2:p.Ala2019Ser
ENST00000346085.10:c.5806G>T	ENSP00000344546.5:p.Ala1936Ser
ENST00000350026.10:c.5518G>T	ENSP00000055163.7:p.Ala1840Ser
ENST00000414678.7:c.4084G>T	ENSP00000412835.2:p.Ala1362Ser
ENST00000635849.1:c.3247G>T	ENSP00000490948.1:p.Ala1083Ser
ENST00000635928.1:c.82G>T	ENSP00000489717.1:p.Ala28Ser
ENST00000635957.1:c.2878G>T	ENSP00000490385.1:p.Ala960Ser
ENST00000636227.1:n.4389G>T
ENST00000636254.1:n.1846G>T
ENST00000636930.2:c.5926G>T MANE Select	ENSP00000490491.2:p.Ala1976Ser
ENST00000636940.1:n.3923G>T
ENST00000637015.1:c.3294G>T
ENST00000637568.1:c.3208G>T
ENST00000637741.1:n.2592G>T
ENST00000637810.1:c.3268G>T	ENSP00000489636.1:p.Ala1090Ser
ENST00000637904.1:c.3427G>T	ENSP00000490550.1:p.Ala1143Ser
ENST00000637933.1:n.3041G>T
ENST00000647938.1:c.5557G>T	ENSP00000498155.1:p.Ala1853Ser
ENST00000346085.9:c.5557G>T	ENSP00000344546.4:p.Ala1853Ser
ENST00000350026.9:c.5518G>T	ENSP00000055163.7:p.Ala1840Ser
ENST00000414678.6:c.4084G>T	ENSP00000412835.2:p.Ala1362Ser
NM_017519.2:c.5518G>T	NP_059989.2:p.Ala1840Ser
NM_020732.3:c.5557G>T	NP_065783.3:p.Ala1853Ser
XM_005267069.3:c.5677G>T	XP_005267126.2:p.Ala1893Ser
XM_011535984.1:c.4756G>T	XP_011534286.1:p.Ala1586Ser
XM_011535985.1:c.4576G>T	XP_011534287.1:p.Ala1526Ser
XM_011535986.1:c.4336G>T	XP_011534288.1:p.Ala1446Ser
XM_011535987.1:c.3955G>T	XP_011534289.1:p.Ala1319Ser
XM_011535988.1:c.2818G>T	XP_011534290.1:p.Ala940Ser
NM_001346813.1:c.5677G>T	NP_001333742.1:p.Ala1893Ser
NM_001363725.1:c.3427G>T	NP_001350654.1:p.Ala1143Ser
XM_011535984.2:c.5887G>T	XP_011534286.2:p.Ala1963Ser
XM_011535988.3:c.2818G>T	XP_011534290.1:p.Ala940Ser
XM_017011103.2:c.5788G>T	XP_016866592.1:p.Ala1930Ser
XM_017011104.1:c.5758G>T	XP_016866593.1:p.Ala1920Ser
XM_017011105.2:c.5728G>T	XP_016866594.1:p.Ala1910Ser
XM_017011106.2:c.5599G>T	XP_016866595.1:p.Ala1867Ser
XM_017011107.2:c.5578G>T	XP_016866596.1:p.Ala1860Ser
XR_002956289.1:n.5873G>T
NM_001363725.2:c.3427G>T	NP_001350654.1:p.Ala1143Ser
NM_001371656.1:c.5806G>T	NP_001358585.1:p.Ala1936Ser
NM_001374820.1:c.5806G>T	NP_001361749.1:p.Ala1936Ser
NM_001374828.1:c.5926G>T MANE Select	NP_001361757.1:p.Ala1976Ser
NM_017519.3:c.5767G>T	NP_059989.3:p.Ala1923Ser