Canonical Allele Identifier: CA1675522794

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200978C= , CM000668.2:g.157200978C=	GRCh38
NC_000006.11:g.157522112C= , CM000668.1:g.157522112C=	GRCh37
NC_000006.10:g.157563804C=	NCBI36
NG_032093.1:g.428049C=
NG_032093.2:g.428049C=
NG_066624.1:g.429953C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4594C=	ENSP00000055163.8:p.Gln1532=
ENST00000414678.8:c.4663C=	ENSP00000412835.3:p.Gln1555=
ENST00000637015.2:c.4882C=	ENSP00000489729.2:p.Gln1628=
ENST00000346085.10:c.4633C=	ENSP00000344546.5:p.Gln1545=
ENST00000350026.10:c.4345C=	ENSP00000055163.7:p.Gln1449=
ENST00000414678.7:c.2911C=	ENSP00000412835.2:p.Gln971=
ENST00000635849.1:c.2074C=	ENSP00000490948.1:p.Gln692=
ENST00000635957.1:c.1705C=	ENSP00000490385.1:p.Gln569=
ENST00000636227.1:n.3216C=
ENST00000636254.1:n.673C=
ENST00000636930.2:c.4753C= MANE Select	ENSP00000490491.2:p.Gln1585=
ENST00000636940.1:n.2750C=
ENST00000637015.1:c.2121C=
ENST00000637568.1:c.2035C=
ENST00000637741.1:n.1419C=
ENST00000637810.1:c.2095C=	ENSP00000489636.1:p.Gln699=
ENST00000637904.1:c.2254C=	ENSP00000490550.1:p.Gln752=
ENST00000647938.1:c.4384C=	ENSP00000498155.1:p.Gln1462=
ENST00000346085.9:c.4384C=	ENSP00000344546.4:p.Gln1462=
ENST00000350026.9:c.4345C=	ENSP00000055163.7:p.Gln1449=
ENST00000414678.6:c.2911C=	ENSP00000412835.2:p.Gln971=
NM_017519.2:c.4345C=	NP_059989.2:p.Gln1449=
NM_020732.3:c.4384C=	NP_065783.3:p.Gln1462=
XM_005267069.3:c.4504C=	XP_005267126.2:p.Gln1502=
XM_011535984.1:c.3583C=	XP_011534286.1:p.Gln1195=
XM_011535985.1:c.3403C=	XP_011534287.1:p.Gln1135=
XM_011535986.1:c.3163C=	XP_011534288.1:p.Gln1055=
XM_011535987.1:c.2782C=	XP_011534289.1:p.Gln928=
XM_011535988.1:c.1645C=	XP_011534290.1:p.Gln549=
NM_001346813.1:c.4504C=	NP_001333742.1:p.Gln1502=
NM_001363725.1:c.2254C=	NP_001350654.1:p.Gln752=
XM_011535984.2:c.4714C=	XP_011534286.2:p.Gln1572=
XM_011535988.3:c.1645C=	XP_011534290.1:p.Gln549=
XM_017011103.2:c.4615C=	XP_016866592.1:p.Gln1539=
XM_017011104.1:c.4585C=	XP_016866593.1:p.Gln1529=
XM_017011105.2:c.4555C=	XP_016866594.1:p.Gln1519=
XM_017011106.2:c.4426C=	XP_016866595.1:p.Gln1476=
XM_017011107.2:c.4405C=	XP_016866596.1:p.Gln1469=
XR_002956289.1:n.4700C=
NM_001363725.2:c.2254C=	NP_001350654.1:p.Gln752=
NM_001371656.1:c.4633C=	NP_001358585.1:p.Gln1545=
NM_001374820.1:c.4633C=	NP_001361749.1:p.Gln1545=
NM_001374828.1:c.4753C= MANE Select	NP_001361757.1:p.Gln1585=
NM_017519.3:c.4594C=	NP_059989.3:p.Gln1532=