Canonical Allele Identifier: CA1675522957

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201089A= , CM000668.2:g.157201089A=	GRCh38
NC_000006.11:g.157522223A= , CM000668.1:g.157522223A=	GRCh37
NC_000006.10:g.157563915A=	NCBI36
NG_032093.1:g.428160A=
NG_032093.2:g.428160A=
NG_066624.1:g.430064A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4705A=	ENSP00000055163.8:p.Met1569=
ENST00000414678.8:c.4774A=	ENSP00000412835.3:p.Met1592=
ENST00000637015.2:c.4993A=	ENSP00000489729.2:p.Met1665=
ENST00000346085.10:c.4744A=	ENSP00000344546.5:p.Met1582=
ENST00000350026.10:c.4456A=	ENSP00000055163.7:p.Met1486=
ENST00000414678.7:c.3022A=	ENSP00000412835.2:p.Met1008=
ENST00000635849.1:c.2185A=	ENSP00000490948.1:p.Met729=
ENST00000635957.1:c.1816A=	ENSP00000490385.1:p.Met606=
ENST00000636227.1:n.3327A=
ENST00000636254.1:n.784A=
ENST00000636930.2:c.4864A= MANE Select	ENSP00000490491.2:p.Met1622=
ENST00000636940.1:n.2861A=
ENST00000637015.1:c.2232A=
ENST00000637568.1:c.2146A=
ENST00000637741.1:n.1530A=
ENST00000637810.1:c.2206A=	ENSP00000489636.1:p.Met736=
ENST00000637904.1:c.2365A=	ENSP00000490550.1:p.Met789=
ENST00000647938.1:c.4495A=	ENSP00000498155.1:p.Met1499=
ENST00000346085.9:c.4495A=	ENSP00000344546.4:p.Met1499=
ENST00000350026.9:c.4456A=	ENSP00000055163.7:p.Met1486=
ENST00000414678.6:c.3022A=	ENSP00000412835.2:p.Met1008=
NM_017519.2:c.4456A=	NP_059989.2:p.Met1486=
NM_020732.3:c.4495A=	NP_065783.3:p.Met1499=
XM_005267069.3:c.4615A=	XP_005267126.2:p.Met1539=
XM_011535984.1:c.3694A=	XP_011534286.1:p.Met1232=
XM_011535985.1:c.3514A=	XP_011534287.1:p.Met1172=
XM_011535986.1:c.3274A=	XP_011534288.1:p.Met1092=
XM_011535987.1:c.2893A=	XP_011534289.1:p.Met965=
XM_011535988.1:c.1756A=	XP_011534290.1:p.Met586=
NM_001346813.1:c.4615A=	NP_001333742.1:p.Met1539=
NM_001363725.1:c.2365A=	NP_001350654.1:p.Met789=
XM_011535984.2:c.4825A=	XP_011534286.2:p.Met1609=
XM_011535988.3:c.1756A=	XP_011534290.1:p.Met586=
XM_017011103.2:c.4726A=	XP_016866592.1:p.Met1576=
XM_017011104.1:c.4696A=	XP_016866593.1:p.Met1566=
XM_017011105.2:c.4666A=	XP_016866594.1:p.Met1556=
XM_017011106.2:c.4537A=	XP_016866595.1:p.Met1513=
XM_017011107.2:c.4516A=	XP_016866596.1:p.Met1506=
XR_002956289.1:n.4811A=
NM_001363725.2:c.2365A=	NP_001350654.1:p.Met789=
NM_001371656.1:c.4744A=	NP_001358585.1:p.Met1582=
NM_001374820.1:c.4744A=	NP_001361749.1:p.Met1582=
NM_001374828.1:c.4864A= MANE Select	NP_001361757.1:p.Met1622=
NM_017519.3:c.4705A=	NP_059989.3:p.Met1569=