Canonical Allele Identifier: CA1675523324

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201283G= , CM000668.2:g.157201283G=	GRCh38
NC_000006.11:g.157522417G= , CM000668.1:g.157522417G=	GRCh37
NC_000006.10:g.157564109G=	NCBI36
NG_032093.1:g.428354G=
NG_032093.2:g.428354G=
NG_066624.1:g.430258G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4899G=	ENSP00000055163.8:p.Leu1633=
ENST00000414678.8:c.4968G=	ENSP00000412835.3:p.Leu1656=
ENST00000637015.2:c.5187G=	ENSP00000489729.2:p.Leu1729=
ENST00000346085.10:c.4938G=	ENSP00000344546.5:p.Leu1646=
ENST00000350026.10:c.4650G=	ENSP00000055163.7:p.Leu1550=
ENST00000414678.7:c.3216G=	ENSP00000412835.2:p.Leu1072=
ENST00000635849.1:c.2379G=	ENSP00000490948.1:p.Leu793=
ENST00000635957.1:c.2010G=	ENSP00000490385.1:p.Leu670=
ENST00000636227.1:n.3521G=
ENST00000636254.1:n.978G=
ENST00000636930.2:c.5058G= MANE Select	ENSP00000490491.2:p.Leu1686=
ENST00000636940.1:n.3055G=
ENST00000637015.1:c.2426G=
ENST00000637568.1:c.2340G=
ENST00000637741.1:n.1724G=
ENST00000637810.1:c.2400G=	ENSP00000489636.1:p.Leu800=
ENST00000637904.1:c.2559G=	ENSP00000490550.1:p.Leu853=
ENST00000647938.1:c.4689G=	ENSP00000498155.1:p.Leu1563=
ENST00000346085.9:c.4689G=	ENSP00000344546.4:p.Leu1563=
ENST00000350026.9:c.4650G=	ENSP00000055163.7:p.Leu1550=
ENST00000414678.6:c.3216G=	ENSP00000412835.2:p.Leu1072=
NM_017519.2:c.4650G=	NP_059989.2:p.Leu1550=
NM_020732.3:c.4689G=	NP_065783.3:p.Leu1563=
XM_005267069.3:c.4809G=	XP_005267126.2:p.Leu1603=
XM_011535984.1:c.3888G=	XP_011534286.1:p.Leu1296=
XM_011535985.1:c.3708G=	XP_011534287.1:p.Leu1236=
XM_011535986.1:c.3468G=	XP_011534288.1:p.Leu1156=
XM_011535987.1:c.3087G=	XP_011534289.1:p.Leu1029=
XM_011535988.1:c.1950G=	XP_011534290.1:p.Leu650=
NM_001346813.1:c.4809G=	NP_001333742.1:p.Leu1603=
NM_001363725.1:c.2559G=	NP_001350654.1:p.Leu853=
XM_011535984.2:c.5019G=	XP_011534286.2:p.Leu1673=
XM_011535988.3:c.1950G=	XP_011534290.1:p.Leu650=
XM_017011103.2:c.4920G=	XP_016866592.1:p.Leu1640=
XM_017011104.1:c.4890G=	XP_016866593.1:p.Leu1630=
XM_017011105.2:c.4860G=	XP_016866594.1:p.Leu1620=
XM_017011106.2:c.4731G=	XP_016866595.1:p.Leu1577=
XM_017011107.2:c.4710G=	XP_016866596.1:p.Leu1570=
XR_002956289.1:n.5005G=
NM_001363725.2:c.2559G=	NP_001350654.1:p.Leu853=
NM_001371656.1:c.4938G=	NP_001358585.1:p.Leu1646=
NM_001374820.1:c.4938G=	NP_001361749.1:p.Leu1646=
NM_001374828.1:c.5058G= MANE Select	NP_001361757.1:p.Leu1686=
NM_017519.3:c.4899G=	NP_059989.3:p.Leu1633=