Canonical Allele Identifier: CA1675542249

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198899C= , CM000668.2:g.157198899C=	GRCh38
NC_000006.11:g.157520033C= , CM000668.1:g.157520033C=	GRCh37
NC_000006.10:g.157561725C=	NCBI36
NG_032093.1:g.425970C=
NG_032093.2:g.425970C=
NG_066624.1:g.427874C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4471C= MANE Select	NP_001361757.1:p.Gln1491=
ENST00000636930.2:c.4471C= MANE Select	ENSP00000490491.2:p.Gln1491=
NM_001346813.1:c.4222C=	NP_001333742.1:p.Gln1408=
NM_001363725.1:c.1972C=	NP_001350654.1:p.Gln658=
NM_001363725.2:c.1972C=	NP_001350654.1:p.Gln658=
NM_001371656.1:c.4351C=	NP_001358585.1:p.Gln1451=
NM_001374820.1:c.4351C=	NP_001361749.1:p.Gln1451=
NM_017519.2:c.4063C=	NP_059989.2:p.Gln1355=
NM_017519.3:c.4312C=	NP_059989.3:p.Gln1438=
NM_020732.3:c.4102C=	NP_065783.3:p.Gln1368=
ENST00000346085.10:c.4351C=	ENSP00000344546.5:p.Gln1451=
ENST00000346085.9:c.4102C=	ENSP00000344546.4:p.Gln1368=
ENST00000350026.10:c.4063C=	ENSP00000055163.7:p.Gln1355=
ENST00000350026.11:c.4312C=	ENSP00000055163.8:p.Gln1438=
ENST00000350026.9:c.4063C=	ENSP00000055163.7:p.Gln1355=
ENST00000414678.6:c.2629C=	ENSP00000412835.2:p.Gln877=
ENST00000414678.7:c.2629C=	ENSP00000412835.2:p.Gln877=
ENST00000414678.8:c.4381C=	ENSP00000412835.3:p.Gln1461=
ENST00000635849.1:c.1792C=	ENSP00000490948.1:p.Gln598=
ENST00000635957.1:c.1423C=	ENSP00000490385.1:p.Gln475=
ENST00000636227.1:n.2934C=
ENST00000636254.1:n.391C=
ENST00000636940.1:n.2468C=
ENST00000637015.1:c.1839C=
ENST00000637015.2:c.4600C=	ENSP00000489729.2:p.Gln1534=
ENST00000637568.1:c.1753C=
ENST00000637741.1:n.1137C=
ENST00000637810.1:c.1813C=	ENSP00000489636.1:p.Gln605=
ENST00000637904.1:c.1972C=	ENSP00000490550.1:p.Gln658=
ENST00000647938.1:c.4102C=	ENSP00000498155.1:p.Gln1368=
XM_005267069.3:c.4222C=	XP_005267126.2:p.Gln1408=
XM_011535984.1:c.3301C=	XP_011534286.1:p.Gln1101=
XM_011535984.2:c.4432C=	XP_011534286.2:p.Gln1478=
XM_011535985.1:c.3121C=	XP_011534287.1:p.Gln1041=
XM_011535986.1:c.2881C=	XP_011534288.1:p.Gln961=
XM_011535987.1:c.2500C=	XP_011534289.1:p.Gln834=
XM_011535988.1:c.1363C=	XP_011534290.1:p.Gln455=
XM_011535988.3:c.1363C=	XP_011534290.1:p.Gln455=
XM_017011103.2:c.4333C=	XP_016866592.1:p.Gln1445=
XM_017011104.1:c.4303C=	XP_016866593.1:p.Gln1435=
XM_017011105.2:c.4273C=	XP_016866594.1:p.Gln1425=
XM_017011106.2:c.4144C=	XP_016866595.1:p.Gln1382=
XM_017011107.2:c.4123C=	XP_016866596.1:p.Gln1375=
XR_002956289.1:n.4427-1806C=