Canonical Allele Identifier: CA1675400809

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901506A= , CM000668.2:g.156901506A=	GRCh38
NC_000006.11:g.157222640A= , CM000668.1:g.157222640A=	GRCh37
NC_000006.10:g.157264332A=	NCBI36
NG_032093.1:g.128577A=
NG_032093.2:g.128577A=
NG_066624.1:g.130481A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2117A=	ENSP00000055163.8:p.Gln706=
ENST00000414678.8:c.2117A=	ENSP00000412835.3:p.Gln706=
ENST00000637015.2:c.2117A=	ENSP00000489729.2:p.Gln706=
ENST00000319584.11:c.131A=	ENSP00000313006.7:p.Gln44=
ENST00000346085.10:c.2156A=	ENSP00000344546.5:p.Gln719=
ENST00000350026.10:c.1868A=	ENSP00000055163.7:p.Gln623=
ENST00000414678.7:c.365A=	ENSP00000412835.2:p.Gln122=
ENST00000636205.1:n.180A=
ENST00000636748.1:c.398A=	ENSP00000489917.1:p.Gln133=
ENST00000636930.2:c.2117A= MANE Select	ENSP00000490491.2:p.Gln706=
ENST00000637532.1:c.143A=	ENSP00000490420.1:p.Gln48=
ENST00000638000.1:c.334A=
ENST00000647938.1:c.1907A=	ENSP00000498155.1:p.Gln636=
ENST00000674190.1:n.824A=
ENST00000674298.1:c.1857A=
ENST00000319584.10:c.134A=	ENSP00000313006.6:p.Gln45=
ENST00000346085.9:c.1907A=	ENSP00000344546.4:p.Gln636=
ENST00000350026.9:c.1868A=	ENSP00000055163.7:p.Gln623=
ENST00000414678.6:c.365A=	ENSP00000412835.2:p.Gln122=
NM_017519.2:c.1868A=	NP_059989.2:p.Gln623=
NM_020732.3:c.1907A=	NP_065783.3:p.Gln636=
XM_005267069.3:c.1868A=	XP_005267126.2:p.Gln623=
XM_011535984.1:c.776A=	XP_011534286.1:p.Gln259=
XM_011535985.1:c.776A=	XP_011534287.1:p.Gln259=
XM_011535986.1:c.356A=	XP_011534288.1:p.Gln119=
NM_001346813.1:c.1868A=	NP_001333742.1:p.Gln623=
XM_011535984.2:c.1907A=	XP_011534286.2:p.Gln636=
XM_017011103.2:c.1907A=	XP_016866592.1:p.Gln636=
XM_017011104.1:c.1907A=	XP_016866593.1:p.Gln636=
XM_017011105.2:c.1907A=	XP_016866594.1:p.Gln636=
XM_017011106.2:c.1907A=	XP_016866595.1:p.Gln636=
XM_017011107.2:c.1907A=	XP_016866596.1:p.Gln636=
XR_002956289.1:n.1990A=
NM_001371656.1:c.2156A=	NP_001358585.1:p.Gln719=
NM_001374820.1:c.2156A=	NP_001361749.1:p.Gln719=
NM_001374828.1:c.2117A= MANE Select	NP_001361757.1:p.Gln706=
NM_017519.3:c.2117A=	NP_059989.3:p.Gln706=