Canonical Allele Identifier: CA1675400808

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901502C= , CM000668.2:g.156901502C=	GRCh38
NC_000006.11:g.157222636C= , CM000668.1:g.157222636C=	GRCh37
NC_000006.10:g.157264328C=	NCBI36
NG_032093.1:g.128573C=
NG_032093.2:g.128573C=
NG_066624.1:g.130477C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2113C=	ENSP00000055163.8:p.Gln705=
ENST00000414678.8:c.2113C=	ENSP00000412835.3:p.Gln705=
ENST00000637015.2:c.2113C=	ENSP00000489729.2:p.Gln705=
ENST00000319584.11:c.127C=	ENSP00000313006.7:p.Gln43=
ENST00000346085.10:c.2152C=	ENSP00000344546.5:p.Gln718=
ENST00000350026.10:c.1864C=	ENSP00000055163.7:p.Gln622=
ENST00000414678.7:c.361C=	ENSP00000412835.2:p.Gln121=
ENST00000636205.1:n.176C=
ENST00000636748.1:c.394C=	ENSP00000489917.1:p.Gln132=
ENST00000636930.2:c.2113C= MANE Select	ENSP00000490491.2:p.Gln705=
ENST00000637532.1:c.139C=	ENSP00000490420.1:p.Gln47=
ENST00000638000.1:c.330C=
ENST00000647938.1:c.1903C=	ENSP00000498155.1:p.Gln635=
ENST00000674190.1:n.820C=
ENST00000674298.1:c.1853C=
ENST00000319584.10:c.130C=	ENSP00000313006.6:p.Gln44=
ENST00000346085.9:c.1903C=	ENSP00000344546.4:p.Gln635=
ENST00000350026.9:c.1864C=	ENSP00000055163.7:p.Gln622=
ENST00000414678.6:c.361C=	ENSP00000412835.2:p.Gln121=
NM_017519.2:c.1864C=	NP_059989.2:p.Gln622=
NM_020732.3:c.1903C=	NP_065783.3:p.Gln635=
XM_005267069.3:c.1864C=	XP_005267126.2:p.Gln622=
XM_011535984.1:c.772C=	XP_011534286.1:p.Gln258=
XM_011535985.1:c.772C=	XP_011534287.1:p.Gln258=
XM_011535986.1:c.352C=	XP_011534288.1:p.Gln118=
NM_001346813.1:c.1864C=	NP_001333742.1:p.Gln622=
XM_011535984.2:c.1903C=	XP_011534286.2:p.Gln635=
XM_017011103.2:c.1903C=	XP_016866592.1:p.Gln635=
XM_017011104.1:c.1903C=	XP_016866593.1:p.Gln635=
XM_017011105.2:c.1903C=	XP_016866594.1:p.Gln635=
XM_017011106.2:c.1903C=	XP_016866595.1:p.Gln635=
XM_017011107.2:c.1903C=	XP_016866596.1:p.Gln635=
XR_002956289.1:n.1986C=
NM_001371656.1:c.2152C=	NP_001358585.1:p.Gln718=
NM_001374820.1:c.2152C=	NP_001361749.1:p.Gln718=
NM_001374828.1:c.2113C= MANE Select	NP_001361757.1:p.Gln705=
NM_017519.3:c.2113C=	NP_059989.3:p.Gln705=