Canonical Allele Identifier: CA1675498995

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157110561G= , CM000668.2:g.157110561G=	GRCh38
NC_000006.11:g.157431695G= , CM000668.1:g.157431695G=	GRCh37
NC_000006.10:g.157473387G=	NCBI36
NG_032093.1:g.337632G=
NG_032093.2:g.337632G=
NG_066624.1:g.339536G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.2581G= MANE Select	NP_001361757.1:p.Gly861=
ENST00000636930.2:c.2581G= MANE Select	ENSP00000490491.2:p.Gly861=
NM_001346813.1:c.2332G=	NP_001333742.1:p.Gly778=
NM_001363725.1:c.82G=	NP_001350654.1:p.Gly28=
NM_001363725.2:c.82G=	NP_001350654.1:p.Gly28=
NM_001371656.1:c.2620G=	NP_001358585.1:p.Gly874=
NM_001374820.1:c.2620G=	NP_001361749.1:p.Gly874=
NM_017519.2:c.2332G=	NP_059989.2:p.Gly778=
NM_017519.3:c.2581G=	NP_059989.3:p.Gly861=
NM_020732.3:c.2371G=	NP_065783.3:p.Gly791=
ENST00000319584.10:c.598G=	ENSP00000313006.6:p.Gly200=
ENST00000319584.11:c.595G=	ENSP00000313006.7:p.Gly199=
ENST00000346085.10:c.2620G=	ENSP00000344546.5:p.Gly874=
ENST00000346085.9:c.2371G=	ENSP00000344546.4:p.Gly791=
ENST00000350026.10:c.2332G=	ENSP00000055163.7:p.Gly778=
ENST00000350026.11:c.2581G=	ENSP00000055163.8:p.Gly861=
ENST00000350026.9:c.2332G=	ENSP00000055163.7:p.Gly778=
ENST00000414678.6:c.740-22467G=	ENSP00000412835.2:n.740-22467G=
ENST00000414678.7:c.740-22467G=	ENSP00000412835.2:n.740-22467G=
ENST00000414678.8:c.2492-22467G=	ENSP00000412835.3:n.2492-22467G=
ENST00000452544.1:n.440G=
ENST00000452544.2:n.482G=
ENST00000493658.1:n.230G=
ENST00000493658.2:n.230G=
ENST00000635849.1:c.82G=	ENSP00000490948.1:p.Gly28=
ENST00000637003.1:c.82G=	ENSP00000489666.1:p.Gly28=
ENST00000637015.2:c.2581G=	ENSP00000489729.2:p.Gly861=
ENST00000637810.1:c.82G=	ENSP00000489636.1:p.Gly28=
ENST00000637904.1:c.82G=	ENSP00000490550.1:p.Gly28=
ENST00000647938.1:c.2371G=	ENSP00000498155.1:p.Gly791=
ENST00000674190.1:n.1330G=
XM_005267069.3:c.2332G=	XP_005267126.2:p.Gly778=
XM_011535984.1:c.1282G=	XP_011534286.1:p.Gly428=
XM_011535984.2:c.2413G=	XP_011534286.2:p.Gly805=
XM_011535985.1:c.1282G=	XP_011534287.1:p.Gly428=
XM_011535986.1:c.862G=	XP_011534288.1:p.Gly288=
XM_011535987.1:c.481G=	XP_011534289.1:p.Gly161=
XM_017011103.2:c.2413G=	XP_016866592.1:p.Gly805=
XM_017011104.1:c.2413G=	XP_016866593.1:p.Gly805=
XM_017011105.2:c.2413G=	XP_016866594.1:p.Gly805=
XM_017011106.2:c.2413G=	XP_016866595.1:p.Gly805=
XM_017011107.2:c.2413G=	XP_016866596.1:p.Gly805=
XR_002956289.1:n.2496G=