Canonical Allele Identifier: CA1675523537

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201390C= , CM000668.2:g.157201390C=	GRCh38
NC_000006.11:g.157522524C= , CM000668.1:g.157522524C=	GRCh37
NC_000006.10:g.157564216C=	NCBI36
NG_032093.1:g.428461C=
NG_032093.2:g.428461C=
NG_066624.1:g.430365C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5006C=	ENSP00000055163.8:p.Pro1669=
ENST00000414678.8:c.5075C=	ENSP00000412835.3:p.Pro1692=
ENST00000637015.2:c.5294C=	ENSP00000489729.2:p.Pro1765=
ENST00000346085.10:c.5045C=	ENSP00000344546.5:p.Pro1682=
ENST00000350026.10:c.4757C=	ENSP00000055163.7:p.Pro1586=
ENST00000414678.7:c.3323C=	ENSP00000412835.2:p.Pro1108=
ENST00000635849.1:c.2486C=	ENSP00000490948.1:p.Pro829=
ENST00000635957.1:c.2117C=	ENSP00000490385.1:p.Pro706=
ENST00000636227.1:n.3628C=
ENST00000636254.1:n.1085C=
ENST00000636930.2:c.5165C= MANE Select	ENSP00000490491.2:p.Pro1722=
ENST00000636940.1:n.3162C=
ENST00000637015.1:c.2533C=
ENST00000637568.1:c.2447C=
ENST00000637741.1:n.1831C=
ENST00000637810.1:c.2507C=	ENSP00000489636.1:p.Pro836=
ENST00000637904.1:c.2666C=	ENSP00000490550.1:p.Pro889=
ENST00000647938.1:c.4796C=	ENSP00000498155.1:p.Pro1599=
ENST00000346085.9:c.4796C=	ENSP00000344546.4:p.Pro1599=
ENST00000350026.9:c.4757C=	ENSP00000055163.7:p.Pro1586=
ENST00000414678.6:c.3323C=	ENSP00000412835.2:p.Pro1108=
NM_017519.2:c.4757C=	NP_059989.2:p.Pro1586=
NM_020732.3:c.4796C=	NP_065783.3:p.Pro1599=
XM_005267069.3:c.4916C=	XP_005267126.2:p.Pro1639=
XM_011535984.1:c.3995C=	XP_011534286.1:p.Pro1332=
XM_011535985.1:c.3815C=	XP_011534287.1:p.Pro1272=
XM_011535986.1:c.3575C=	XP_011534288.1:p.Pro1192=
XM_011535987.1:c.3194C=	XP_011534289.1:p.Pro1065=
XM_011535988.1:c.2057C=	XP_011534290.1:p.Pro686=
NM_001346813.1:c.4916C=	NP_001333742.1:p.Pro1639=
NM_001363725.1:c.2666C=	NP_001350654.1:p.Pro889=
XM_011535984.2:c.5126C=	XP_011534286.2:p.Pro1709=
XM_011535988.3:c.2057C=	XP_011534290.1:p.Pro686=
XM_017011103.2:c.5027C=	XP_016866592.1:p.Pro1676=
XM_017011104.1:c.4997C=	XP_016866593.1:p.Pro1666=
XM_017011105.2:c.4967C=	XP_016866594.1:p.Pro1656=
XM_017011106.2:c.4838C=	XP_016866595.1:p.Pro1613=
XM_017011107.2:c.4817C=	XP_016866596.1:p.Pro1606=
XR_002956289.1:n.5112C=
NM_001363725.2:c.2666C=	NP_001350654.1:p.Pro889=
NM_001371656.1:c.5045C=	NP_001358585.1:p.Pro1682=
NM_001374820.1:c.5045C=	NP_001361749.1:p.Pro1682=
NM_001374828.1:c.5165C= MANE Select	NP_001361757.1:p.Pro1722=
NM_017519.3:c.5006C=	NP_059989.3:p.Pro1669=