Canonical Allele Identifier: CA1675523332

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201290C= , CM000668.2:g.157201290C=	GRCh38
NC_000006.11:g.157522424C= , CM000668.1:g.157522424C=	GRCh37
NC_000006.10:g.157564116C=	NCBI36
NG_032093.1:g.428361C=
NG_032093.2:g.428361C=
NG_066624.1:g.430265C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4906C=	ENSP00000055163.8:p.Arg1636=
ENST00000414678.8:c.4975C=	ENSP00000412835.3:p.Arg1659=
ENST00000637015.2:c.5194C=	ENSP00000489729.2:p.Arg1732=
ENST00000346085.10:c.4945C=	ENSP00000344546.5:p.Arg1649=
ENST00000350026.10:c.4657C=	ENSP00000055163.7:p.Arg1553=
ENST00000414678.7:c.3223C=	ENSP00000412835.2:p.Arg1075=
ENST00000635849.1:c.2386C=	ENSP00000490948.1:p.Arg796=
ENST00000635957.1:c.2017C=	ENSP00000490385.1:p.Arg673=
ENST00000636227.1:n.3528C=
ENST00000636254.1:n.985C=
ENST00000636930.2:c.5065C= MANE Select	ENSP00000490491.2:p.Arg1689=
ENST00000636940.1:n.3062C=
ENST00000637015.1:c.2433C=
ENST00000637568.1:c.2347C=
ENST00000637741.1:n.1731C=
ENST00000637810.1:c.2407C=	ENSP00000489636.1:p.Arg803=
ENST00000637904.1:c.2566C=	ENSP00000490550.1:p.Arg856=
ENST00000647938.1:c.4696C=	ENSP00000498155.1:p.Arg1566=
ENST00000346085.9:c.4696C=	ENSP00000344546.4:p.Arg1566=
ENST00000350026.9:c.4657C=	ENSP00000055163.7:p.Arg1553=
ENST00000414678.6:c.3223C=	ENSP00000412835.2:p.Arg1075=
NM_017519.2:c.4657C=	NP_059989.2:p.Arg1553=
NM_020732.3:c.4696C=	NP_065783.3:p.Arg1566=
XM_005267069.3:c.4816C=	XP_005267126.2:p.Arg1606=
XM_011535984.1:c.3895C=	XP_011534286.1:p.Arg1299=
XM_011535985.1:c.3715C=	XP_011534287.1:p.Arg1239=
XM_011535986.1:c.3475C=	XP_011534288.1:p.Arg1159=
XM_011535987.1:c.3094C=	XP_011534289.1:p.Arg1032=
XM_011535988.1:c.1957C=	XP_011534290.1:p.Arg653=
NM_001346813.1:c.4816C=	NP_001333742.1:p.Arg1606=
NM_001363725.1:c.2566C=	NP_001350654.1:p.Arg856=
XM_011535984.2:c.5026C=	XP_011534286.2:p.Arg1676=
XM_011535988.3:c.1957C=	XP_011534290.1:p.Arg653=
XM_017011103.2:c.4927C=	XP_016866592.1:p.Arg1643=
XM_017011104.1:c.4897C=	XP_016866593.1:p.Arg1633=
XM_017011105.2:c.4867C=	XP_016866594.1:p.Arg1623=
XM_017011106.2:c.4738C=	XP_016866595.1:p.Arg1580=
XM_017011107.2:c.4717C=	XP_016866596.1:p.Arg1573=
XR_002956289.1:n.5012C=
NM_001363725.2:c.2566C=	NP_001350654.1:p.Arg856=
NM_001371656.1:c.4945C=	NP_001358585.1:p.Arg1649=
NM_001374820.1:c.4945C=	NP_001361749.1:p.Arg1649=
NM_001374828.1:c.5065C= MANE Select	NP_001361757.1:p.Arg1689=
NM_017519.3:c.4906C=	NP_059989.3:p.Arg1636=