Canonical Allele Identifier: CA1675523369

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201305A= , CM000668.2:g.157201305A=	GRCh38
NC_000006.11:g.157522439A= , CM000668.1:g.157522439A=	GRCh37
NC_000006.10:g.157564131A=	NCBI36
NG_032093.1:g.428376A=
NG_032093.2:g.428376A=
NG_066624.1:g.430280A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4921A=	ENSP00000055163.8:p.Lys1641=
ENST00000414678.8:c.4990A=	ENSP00000412835.3:p.Lys1664=
ENST00000637015.2:c.5209A=	ENSP00000489729.2:p.Lys1737=
ENST00000346085.10:c.4960A=	ENSP00000344546.5:p.Lys1654=
ENST00000350026.10:c.4672A=	ENSP00000055163.7:p.Lys1558=
ENST00000414678.7:c.3238A=	ENSP00000412835.2:p.Lys1080=
ENST00000635849.1:c.2401A=	ENSP00000490948.1:p.Lys801=
ENST00000635957.1:c.2032A=	ENSP00000490385.1:p.Lys678=
ENST00000636227.1:n.3543A=
ENST00000636254.1:n.1000A=
ENST00000636930.2:c.5080A= MANE Select	ENSP00000490491.2:p.Lys1694=
ENST00000636940.1:n.3077A=
ENST00000637015.1:c.2448A=
ENST00000637568.1:c.2362A=
ENST00000637741.1:n.1746A=
ENST00000637810.1:c.2422A=	ENSP00000489636.1:p.Lys808=
ENST00000637904.1:c.2581A=	ENSP00000490550.1:p.Lys861=
ENST00000647938.1:c.4711A=	ENSP00000498155.1:p.Lys1571=
ENST00000346085.9:c.4711A=	ENSP00000344546.4:p.Lys1571=
ENST00000350026.9:c.4672A=	ENSP00000055163.7:p.Lys1558=
ENST00000414678.6:c.3238A=	ENSP00000412835.2:p.Lys1080=
NM_017519.2:c.4672A=	NP_059989.2:p.Lys1558=
NM_020732.3:c.4711A=	NP_065783.3:p.Lys1571=
XM_005267069.3:c.4831A=	XP_005267126.2:p.Lys1611=
XM_011535984.1:c.3910A=	XP_011534286.1:p.Lys1304=
XM_011535985.1:c.3730A=	XP_011534287.1:p.Lys1244=
XM_011535986.1:c.3490A=	XP_011534288.1:p.Lys1164=
XM_011535987.1:c.3109A=	XP_011534289.1:p.Lys1037=
XM_011535988.1:c.1972A=	XP_011534290.1:p.Lys658=
NM_001346813.1:c.4831A=	NP_001333742.1:p.Lys1611=
NM_001363725.1:c.2581A=	NP_001350654.1:p.Lys861=
XM_011535984.2:c.5041A=	XP_011534286.2:p.Lys1681=
XM_011535988.3:c.1972A=	XP_011534290.1:p.Lys658=
XM_017011103.2:c.4942A=	XP_016866592.1:p.Lys1648=
XM_017011104.1:c.4912A=	XP_016866593.1:p.Lys1638=
XM_017011105.2:c.4882A=	XP_016866594.1:p.Lys1628=
XM_017011106.2:c.4753A=	XP_016866595.1:p.Lys1585=
XM_017011107.2:c.4732A=	XP_016866596.1:p.Lys1578=
XR_002956289.1:n.5027A=
NM_001363725.2:c.2581A=	NP_001350654.1:p.Lys861=
NM_001371656.1:c.4960A=	NP_001358585.1:p.Lys1654=
NM_001374820.1:c.4960A=	NP_001361749.1:p.Lys1654=
NM_001374828.1:c.5080A= MANE Select	NP_001361757.1:p.Lys1694=
NM_017519.3:c.4921A=	NP_059989.3:p.Lys1641=