Canonical Allele Identifier: CA1675523301

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201279C= , CM000668.2:g.157201279C=	GRCh38
NC_000006.11:g.157522413C= , CM000668.1:g.157522413C=	GRCh37
NC_000006.10:g.157564105C=	NCBI36
NG_032093.1:g.428350C=
NG_032093.2:g.428350C=
NG_066624.1:g.430254C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4895C=	ENSP00000055163.8:p.Ser1632=
ENST00000414678.8:c.4964C=	ENSP00000412835.3:p.Ser1655=
ENST00000637015.2:c.5183C=	ENSP00000489729.2:p.Ser1728=
ENST00000346085.10:c.4934C=	ENSP00000344546.5:p.Ser1645=
ENST00000350026.10:c.4646C=	ENSP00000055163.7:p.Ser1549=
ENST00000414678.7:c.3212C=	ENSP00000412835.2:p.Ser1071=
ENST00000635849.1:c.2375C=	ENSP00000490948.1:p.Ser792=
ENST00000635957.1:c.2006C=	ENSP00000490385.1:p.Ser669=
ENST00000636227.1:n.3517C=
ENST00000636254.1:n.974C=
ENST00000636930.2:c.5054C= MANE Select	ENSP00000490491.2:p.Ser1685=
ENST00000636940.1:n.3051C=
ENST00000637015.1:c.2422C=
ENST00000637568.1:c.2336C=
ENST00000637741.1:n.1720C=
ENST00000637810.1:c.2396C=	ENSP00000489636.1:p.Ser799=
ENST00000637904.1:c.2555C=	ENSP00000490550.1:p.Ser852=
ENST00000647938.1:c.4685C=	ENSP00000498155.1:p.Ser1562=
ENST00000346085.9:c.4685C=	ENSP00000344546.4:p.Ser1562=
ENST00000350026.9:c.4646C=	ENSP00000055163.7:p.Ser1549=
ENST00000414678.6:c.3212C=	ENSP00000412835.2:p.Ser1071=
NM_017519.2:c.4646C=	NP_059989.2:p.Ser1549=
NM_020732.3:c.4685C=	NP_065783.3:p.Ser1562=
XM_005267069.3:c.4805C=	XP_005267126.2:p.Ser1602=
XM_011535984.1:c.3884C=	XP_011534286.1:p.Ser1295=
XM_011535985.1:c.3704C=	XP_011534287.1:p.Ser1235=
XM_011535986.1:c.3464C=	XP_011534288.1:p.Ser1155=
XM_011535987.1:c.3083C=	XP_011534289.1:p.Ser1028=
XM_011535988.1:c.1946C=	XP_011534290.1:p.Ser649=
NM_001346813.1:c.4805C=	NP_001333742.1:p.Ser1602=
NM_001363725.1:c.2555C=	NP_001350654.1:p.Ser852=
XM_011535984.2:c.5015C=	XP_011534286.2:p.Ser1672=
XM_011535988.3:c.1946C=	XP_011534290.1:p.Ser649=
XM_017011103.2:c.4916C=	XP_016866592.1:p.Ser1639=
XM_017011104.1:c.4886C=	XP_016866593.1:p.Ser1629=
XM_017011105.2:c.4856C=	XP_016866594.1:p.Ser1619=
XM_017011106.2:c.4727C=	XP_016866595.1:p.Ser1576=
XM_017011107.2:c.4706C=	XP_016866596.1:p.Ser1569=
XR_002956289.1:n.5001C=
NM_001363725.2:c.2555C=	NP_001350654.1:p.Ser852=
NM_001371656.1:c.4934C=	NP_001358585.1:p.Ser1645=
NM_001374820.1:c.4934C=	NP_001361749.1:p.Ser1645=
NM_001374828.1:c.5054C= MANE Select	NP_001361757.1:p.Ser1685=
NM_017519.3:c.4895C=	NP_059989.3:p.Ser1632=