Canonical Allele Identifier: CA1675543208

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207241C= , CM000668.2:g.157207241C=	GRCh38
NC_000006.11:g.157528375C= , CM000668.1:g.157528375C=	GRCh37
NC_000006.10:g.157570067C=	NCBI36
NG_032093.1:g.434312C=
NG_032093.2:g.434312C=
NG_066624.1:g.436216C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.6469C= MANE Select	NP_001361757.1:p.Gln2157=
ENST00000636930.2:c.6469C= MANE Select	ENSP00000490491.2:p.Gln2157=
NM_001346813.1:c.6220C=	NP_001333742.1:p.Gln2074=
NM_001363725.1:c.3970C=	NP_001350654.1:p.Gln1324=
NM_001363725.2:c.3970C=	NP_001350654.1:p.Gln1324=
NM_001371656.1:c.6349C=	NP_001358585.1:p.Gln2117=
NM_001374820.1:c.6349C=	NP_001361749.1:p.Gln2117=
NM_017519.2:c.6061C=	NP_059989.2:p.Gln2021=
NM_017519.3:c.6310C=	NP_059989.3:p.Gln2104=
NM_020732.3:c.6100C=	NP_065783.3:p.Gln2034=
ENST00000346085.10:c.6349C=	ENSP00000344546.5:p.Gln2117=
ENST00000346085.9:c.6100C=	ENSP00000344546.4:p.Gln2034=
ENST00000350026.10:c.6061C=	ENSP00000055163.7:p.Gln2021=
ENST00000350026.11:c.6310C=	ENSP00000055163.8:p.Gln2104=
ENST00000350026.9:c.6061C=	ENSP00000055163.7:p.Gln2021=
ENST00000414678.6:c.4627C=	ENSP00000412835.2:p.Gln1543=
ENST00000414678.7:c.4627C=	ENSP00000412835.2:p.Gln1543=
ENST00000414678.8:c.6379C=	ENSP00000412835.3:p.Gln2127=
ENST00000635849.1:c.3790C=	ENSP00000490948.1:p.Gln1264=
ENST00000635928.1:c.625C=	ENSP00000489717.1:p.Gln209=
ENST00000635957.1:c.3421C=	ENSP00000490385.1:p.Gln1141=
ENST00000636227.1:n.4932C=
ENST00000636254.1:n.2389C=
ENST00000636940.1:n.4466C=
ENST00000637015.1:c.3837C=
ENST00000637015.2:c.6598C=	ENSP00000489729.2:p.Gln2200=
ENST00000637568.1:c.3751C=
ENST00000637741.1:n.3135C=
ENST00000637810.1:c.3811C=	ENSP00000489636.1:p.Gln1271=
ENST00000637904.1:c.3970C=	ENSP00000490550.1:p.Gln1324=
ENST00000637933.1:n.3584C=
ENST00000647938.1:c.6100C=	ENSP00000498155.1:p.Gln2034=
XM_005267069.3:c.6220C=	XP_005267126.2:p.Gln2074=
XM_011535984.1:c.5299C=	XP_011534286.1:p.Gln1767=
XM_011535984.2:c.6430C=	XP_011534286.2:p.Gln2144=
XM_011535985.1:c.5119C=	XP_011534287.1:p.Gln1707=
XM_011535986.1:c.4879C=	XP_011534288.1:p.Gln1627=
XM_011535987.1:c.4498C=	XP_011534289.1:p.Gln1500=
XM_011535988.1:c.3361C=	XP_011534290.1:p.Gln1121=
XM_011535988.3:c.3361C=	XP_011534290.1:p.Gln1121=
XM_017011103.2:c.6331C=	XP_016866592.1:p.Gln2111=
XM_017011104.1:c.6301C=	XP_016866593.1:p.Gln2101=
XM_017011105.2:c.6271C=	XP_016866594.1:p.Gln2091=
XM_017011106.2:c.6142C=	XP_016866595.1:p.Gln2048=
XM_017011107.2:c.6121C=	XP_016866596.1:p.Gln2041=
XR_002956289.1:n.6416C=