Canonical Allele Identifier: CA1675522820

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201029C= , CM000668.2:g.157201029C=	GRCh38
NC_000006.11:g.157522163C= , CM000668.1:g.157522163C=	GRCh37
NC_000006.10:g.157563855C=	NCBI36
NG_032093.1:g.428100C=
NG_032093.2:g.428100C=
NG_066624.1:g.430004C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4645C=	ENSP00000055163.8:p.Gln1549=
ENST00000414678.8:c.4714C=	ENSP00000412835.3:p.Gln1572=
ENST00000637015.2:c.4933C=	ENSP00000489729.2:p.Gln1645=
ENST00000346085.10:c.4684C=	ENSP00000344546.5:p.Gln1562=
ENST00000350026.10:c.4396C=	ENSP00000055163.7:p.Gln1466=
ENST00000414678.7:c.2962C=	ENSP00000412835.2:p.Gln988=
ENST00000635849.1:c.2125C=	ENSP00000490948.1:p.Gln709=
ENST00000635957.1:c.1756C=	ENSP00000490385.1:p.Gln586=
ENST00000636227.1:n.3267C=
ENST00000636254.1:n.724C=
ENST00000636930.2:c.4804C= MANE Select	ENSP00000490491.2:p.Gln1602=
ENST00000636940.1:n.2801C=
ENST00000637015.1:c.2172C=
ENST00000637568.1:c.2086C=
ENST00000637741.1:n.1470C=
ENST00000637810.1:c.2146C=	ENSP00000489636.1:p.Gln716=
ENST00000637904.1:c.2305C=	ENSP00000490550.1:p.Gln769=
ENST00000647938.1:c.4435C=	ENSP00000498155.1:p.Gln1479=
ENST00000346085.9:c.4435C=	ENSP00000344546.4:p.Gln1479=
ENST00000350026.9:c.4396C=	ENSP00000055163.7:p.Gln1466=
ENST00000414678.6:c.2962C=	ENSP00000412835.2:p.Gln988=
NM_017519.2:c.4396C=	NP_059989.2:p.Gln1466=
NM_020732.3:c.4435C=	NP_065783.3:p.Gln1479=
XM_005267069.3:c.4555C=	XP_005267126.2:p.Gln1519=
XM_011535984.1:c.3634C=	XP_011534286.1:p.Gln1212=
XM_011535985.1:c.3454C=	XP_011534287.1:p.Gln1152=
XM_011535986.1:c.3214C=	XP_011534288.1:p.Gln1072=
XM_011535987.1:c.2833C=	XP_011534289.1:p.Gln945=
XM_011535988.1:c.1696C=	XP_011534290.1:p.Gln566=
NM_001346813.1:c.4555C=	NP_001333742.1:p.Gln1519=
NM_001363725.1:c.2305C=	NP_001350654.1:p.Gln769=
XM_011535984.2:c.4765C=	XP_011534286.2:p.Gln1589=
XM_011535988.3:c.1696C=	XP_011534290.1:p.Gln566=
XM_017011103.2:c.4666C=	XP_016866592.1:p.Gln1556=
XM_017011104.1:c.4636C=	XP_016866593.1:p.Gln1546=
XM_017011105.2:c.4606C=	XP_016866594.1:p.Gln1536=
XM_017011106.2:c.4477C=	XP_016866595.1:p.Gln1493=
XM_017011107.2:c.4456C=	XP_016866596.1:p.Gln1486=
XR_002956289.1:n.4751C=
NM_001363725.2:c.2305C=	NP_001350654.1:p.Gln769=
NM_001371656.1:c.4684C=	NP_001358585.1:p.Gln1562=
NM_001374820.1:c.4684C=	NP_001361749.1:p.Gln1562=
NM_001374828.1:c.4804C= MANE Select	NP_001361757.1:p.Gln1602=
NM_017519.3:c.4645C=	NP_059989.3:p.Gln1549=