Canonical Allele Identifier: CA366247832

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207008C>T , CM000668.2:g.157207008C>T	GRCh38
NC_000006.11:g.157528142C>T , CM000668.1:g.157528142C>T	GRCh37
NC_000006.10:g.157569834C>T	NCBI36
NG_032093.1:g.434079C>T
NG_032093.2:g.434079C>T
NG_066624.1:g.435983C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.6077C>T	ENSP00000055163.8:p.Ser2026Leu
ENST00000414678.8:c.6146C>T	ENSP00000412835.3:p.Ser2049Leu
ENST00000637015.2:c.6365C>T	ENSP00000489729.2:p.Ser2122Leu
ENST00000346085.10:c.6116C>T	ENSP00000344546.5:p.Ser2039Leu
ENST00000350026.10:c.5828C>T	ENSP00000055163.7:p.Ser1943Leu
ENST00000414678.7:c.4394C>T	ENSP00000412835.2:p.Ser1465Leu
ENST00000635849.1:c.3557C>T	ENSP00000490948.1:p.Ser1186Leu
ENST00000635928.1:c.392C>T	ENSP00000489717.1:p.Ser131Leu
ENST00000635957.1:c.3188C>T	ENSP00000490385.1:p.Ser1063Leu
ENST00000636227.1:n.4699C>T
ENST00000636254.1:n.2156C>T
ENST00000636930.2:c.6236C>T MANE Select	ENSP00000490491.2:p.Ser2079Leu
ENST00000636940.1:n.4233C>T
ENST00000637015.1:c.3604C>T
ENST00000637568.1:c.3518C>T
ENST00000637741.1:n.2902C>T
ENST00000637810.1:c.3578C>T	ENSP00000489636.1:p.Ser1193Leu
ENST00000637904.1:c.3737C>T	ENSP00000490550.1:p.Ser1246Leu
ENST00000637933.1:n.3351C>T
ENST00000647938.1:c.5867C>T	ENSP00000498155.1:p.Ser1956Leu
ENST00000346085.9:c.5867C>T	ENSP00000344546.4:p.Ser1956Leu
ENST00000350026.9:c.5828C>T	ENSP00000055163.7:p.Ser1943Leu
ENST00000414678.6:c.4394C>T	ENSP00000412835.2:p.Ser1465Leu
NM_017519.2:c.5828C>T	NP_059989.2:p.Ser1943Leu
NM_020732.3:c.5867C>T	NP_065783.3:p.Ser1956Leu
XM_005267069.3:c.5987C>T	XP_005267126.2:p.Ser1996Leu
XM_011535984.1:c.5066C>T	XP_011534286.1:p.Ser1689Leu
XM_011535985.1:c.4886C>T	XP_011534287.1:p.Ser1629Leu
XM_011535986.1:c.4646C>T	XP_011534288.1:p.Ser1549Leu
XM_011535987.1:c.4265C>T	XP_011534289.1:p.Ser1422Leu
XM_011535988.1:c.3128C>T	XP_011534290.1:p.Ser1043Leu
NM_001346813.1:c.5987C>T	NP_001333742.1:p.Ser1996Leu
NM_001363725.1:c.3737C>T	NP_001350654.1:p.Ser1246Leu
XM_011535984.2:c.6197C>T	XP_011534286.2:p.Ser2066Leu
XM_011535988.3:c.3128C>T	XP_011534290.1:p.Ser1043Leu
XM_017011103.2:c.6098C>T	XP_016866592.1:p.Ser2033Leu
XM_017011104.1:c.6068C>T	XP_016866593.1:p.Ser2023Leu
XM_017011105.2:c.6038C>T	XP_016866594.1:p.Ser2013Leu
XM_017011106.2:c.5909C>T	XP_016866595.1:p.Ser1970Leu
XM_017011107.2:c.5888C>T	XP_016866596.1:p.Ser1963Leu
XR_002956289.1:n.6183C>T
NM_001363725.2:c.3737C>T	NP_001350654.1:p.Ser1246Leu
NM_001371656.1:c.6116C>T	NP_001358585.1:p.Ser2039Leu
NM_001374820.1:c.6116C>T	NP_001361749.1:p.Ser2039Leu
NM_001374828.1:c.6236C>T MANE Select	NP_001361757.1:p.Ser2079Leu
NM_017519.3:c.6077C>T	NP_059989.3:p.Ser2026Leu