Canonical Allele Identifier: CA366248481

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207301C>T , CM000668.2:g.157207301C>T	GRCh38
NC_000006.11:g.157528435C>T , CM000668.1:g.157528435C>T	GRCh37
NC_000006.10:g.157570127C>T	NCBI36
NG_032093.1:g.434372C>T
NG_032093.2:g.434372C>T
NG_066624.1:g.436276C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.6370C>T	ENSP00000055163.8:p.His2124Tyr
ENST00000414678.8:c.6439C>T	ENSP00000412835.3:p.His2147Tyr
ENST00000637015.2:c.6658C>T	ENSP00000489729.2:p.His2220Tyr
ENST00000346085.10:c.6409C>T	ENSP00000344546.5:p.His2137Tyr
ENST00000350026.10:c.6121C>T	ENSP00000055163.7:p.His2041Tyr
ENST00000414678.7:c.4687C>T	ENSP00000412835.2:p.His1563Tyr
ENST00000635849.1:c.3850C>T	ENSP00000490948.1:p.His1284Tyr
ENST00000635928.1:c.685C>T	ENSP00000489717.1:p.His229Tyr
ENST00000635957.1:c.3481C>T	ENSP00000490385.1:p.His1161Tyr
ENST00000636227.1:n.4992C>T
ENST00000636254.1:n.2449C>T
ENST00000636930.2:c.6529C>T MANE Select	ENSP00000490491.2:p.His2177Tyr
ENST00000636940.1:n.4526C>T
ENST00000637015.1:c.3897C>T
ENST00000637568.1:c.3811C>T
ENST00000637741.1:n.3195C>T
ENST00000637810.1:c.3871C>T	ENSP00000489636.1:p.His1291Tyr
ENST00000637904.1:c.4030C>T	ENSP00000490550.1:p.His1344Tyr
ENST00000637933.1:n.3644C>T
ENST00000647938.1:c.6160C>T	ENSP00000498155.1:p.His2054Tyr
ENST00000346085.9:c.6160C>T	ENSP00000344546.4:p.His2054Tyr
ENST00000350026.9:c.6121C>T	ENSP00000055163.7:p.His2041Tyr
ENST00000414678.6:c.4687C>T	ENSP00000412835.2:p.His1563Tyr
NM_017519.2:c.6121C>T	NP_059989.2:p.His2041Tyr
NM_020732.3:c.6160C>T	NP_065783.3:p.His2054Tyr
XM_005267069.3:c.6280C>T	XP_005267126.2:p.His2094Tyr
XM_011535984.1:c.5359C>T	XP_011534286.1:p.His1787Tyr
XM_011535985.1:c.5179C>T	XP_011534287.1:p.His1727Tyr
XM_011535986.1:c.4939C>T	XP_011534288.1:p.His1647Tyr
XM_011535987.1:c.4558C>T	XP_011534289.1:p.His1520Tyr
XM_011535988.1:c.3421C>T	XP_011534290.1:p.His1141Tyr
NM_001346813.1:c.6280C>T	NP_001333742.1:p.His2094Tyr
NM_001363725.1:c.4030C>T	NP_001350654.1:p.His1344Tyr
XM_011535984.2:c.6490C>T	XP_011534286.2:p.His2164Tyr
XM_011535988.3:c.3421C>T	XP_011534290.1:p.His1141Tyr
XM_017011103.2:c.6391C>T	XP_016866592.1:p.His2131Tyr
XM_017011104.1:c.6361C>T	XP_016866593.1:p.His2121Tyr
XM_017011105.2:c.6331C>T	XP_016866594.1:p.His2111Tyr
XM_017011106.2:c.6202C>T	XP_016866595.1:p.His2068Tyr
XM_017011107.2:c.6181C>T	XP_016866596.1:p.His2061Tyr
XR_002956289.1:n.6476C>T
NM_001363725.2:c.4030C>T	NP_001350654.1:p.His1344Tyr
NM_001371656.1:c.6409C>T	NP_001358585.1:p.His2137Tyr
NM_001374820.1:c.6409C>T	NP_001361749.1:p.His2137Tyr
NM_001374828.1:c.6529C>T MANE Select	NP_001361757.1:p.His2177Tyr
NM_017519.3:c.6370C>T	NP_059989.3:p.His2124Tyr