Canonical Allele Identifier: CA1675543150

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200930C= , CM000668.2:g.157200930C=	GRCh38
NC_000006.11:g.157522064C= , CM000668.1:g.157522064C=	GRCh37
NC_000006.10:g.157563756C=	NCBI36
NG_032093.1:g.428001C=
NG_032093.2:g.428001C=
NG_066624.1:g.429905C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4705C= MANE Select	NP_001361757.1:p.Gln1569=
ENST00000636930.2:c.4705C= MANE Select	ENSP00000490491.2:p.Gln1569=
NM_001346813.1:c.4456C=	NP_001333742.1:p.Gln1486=
NM_001363725.1:c.2206C=	NP_001350654.1:p.Gln736=
NM_001363725.2:c.2206C=	NP_001350654.1:p.Gln736=
NM_001371656.1:c.4585C=	NP_001358585.1:p.Gln1529=
NM_001374820.1:c.4585C=	NP_001361749.1:p.Gln1529=
NM_017519.2:c.4297C=	NP_059989.2:p.Gln1433=
NM_017519.3:c.4546C=	NP_059989.3:p.Gln1516=
NM_020732.3:c.4336C=	NP_065783.3:p.Gln1446=
ENST00000346085.10:c.4585C=	ENSP00000344546.5:p.Gln1529=
ENST00000346085.9:c.4336C=	ENSP00000344546.4:p.Gln1446=
ENST00000350026.10:c.4297C=	ENSP00000055163.7:p.Gln1433=
ENST00000350026.11:c.4546C=	ENSP00000055163.8:p.Gln1516=
ENST00000350026.9:c.4297C=	ENSP00000055163.7:p.Gln1433=
ENST00000414678.6:c.2863C=	ENSP00000412835.2:p.Gln955=
ENST00000414678.7:c.2863C=	ENSP00000412835.2:p.Gln955=
ENST00000414678.8:c.4615C=	ENSP00000412835.3:p.Gln1539=
ENST00000635849.1:c.2026C=	ENSP00000490948.1:p.Gln676=
ENST00000635957.1:c.1657C=	ENSP00000490385.1:p.Gln553=
ENST00000636227.1:n.3168C=
ENST00000636254.1:n.625C=
ENST00000636940.1:n.2702C=
ENST00000637015.1:c.2073C=
ENST00000637015.2:c.4834C=	ENSP00000489729.2:p.Gln1612=
ENST00000637568.1:c.1987C=
ENST00000637741.1:n.1371C=
ENST00000637810.1:c.2047C=	ENSP00000489636.1:p.Gln683=
ENST00000637904.1:c.2206C=	ENSP00000490550.1:p.Gln736=
ENST00000647938.1:c.4336C=	ENSP00000498155.1:p.Gln1446=
XM_005267069.3:c.4456C=	XP_005267126.2:p.Gln1486=
XM_011535984.1:c.3535C=	XP_011534286.1:p.Gln1179=
XM_011535984.2:c.4666C=	XP_011534286.2:p.Gln1556=
XM_011535985.1:c.3355C=	XP_011534287.1:p.Gln1119=
XM_011535986.1:c.3115C=	XP_011534288.1:p.Gln1039=
XM_011535987.1:c.2734C=	XP_011534289.1:p.Gln912=
XM_011535988.1:c.1597C=	XP_011534290.1:p.Gln533=
XM_011535988.3:c.1597C=	XP_011534290.1:p.Gln533=
XM_017011103.2:c.4567C=	XP_016866592.1:p.Gln1523=
XM_017011104.1:c.4537C=	XP_016866593.1:p.Gln1513=
XM_017011105.2:c.4507C=	XP_016866594.1:p.Gln1503=
XM_017011106.2:c.4378C=	XP_016866595.1:p.Gln1460=
XM_017011107.2:c.4357C=	XP_016866596.1:p.Gln1453=
XR_002956289.1:n.4652C=