Canonical Allele Identifier: CA1675523416

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201328G= , CM000668.2:g.157201328G=	GRCh38
NC_000006.11:g.157522462G= , CM000668.1:g.157522462G=	GRCh37
NC_000006.10:g.157564154G=	NCBI36
NG_032093.1:g.428399G=
NG_032093.2:g.428399G=
NG_066624.1:g.430303G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4944G=	ENSP00000055163.8:p.Met1648=
ENST00000414678.8:c.5013G=	ENSP00000412835.3:p.Met1671=
ENST00000637015.2:c.5232G=	ENSP00000489729.2:p.Met1744=
ENST00000346085.10:c.4983G=	ENSP00000344546.5:p.Met1661=
ENST00000350026.10:c.4695G=	ENSP00000055163.7:p.Met1565=
ENST00000414678.7:c.3261G=	ENSP00000412835.2:p.Met1087=
ENST00000635849.1:c.2424G=	ENSP00000490948.1:p.Met808=
ENST00000635957.1:c.2055G=	ENSP00000490385.1:p.Met685=
ENST00000636227.1:n.3566G=
ENST00000636254.1:n.1023G=
ENST00000636930.2:c.5103G= MANE Select	ENSP00000490491.2:p.Met1701=
ENST00000636940.1:n.3100G=
ENST00000637015.1:c.2471G=
ENST00000637568.1:c.2385G=
ENST00000637741.1:n.1769G=
ENST00000637810.1:c.2445G=	ENSP00000489636.1:p.Met815=
ENST00000637904.1:c.2604G=	ENSP00000490550.1:p.Met868=
ENST00000647938.1:c.4734G=	ENSP00000498155.1:p.Met1578=
ENST00000346085.9:c.4734G=	ENSP00000344546.4:p.Met1578=
ENST00000350026.9:c.4695G=	ENSP00000055163.7:p.Met1565=
ENST00000414678.6:c.3261G=	ENSP00000412835.2:p.Met1087=
NM_017519.2:c.4695G=	NP_059989.2:p.Met1565=
NM_020732.3:c.4734G=	NP_065783.3:p.Met1578=
XM_005267069.3:c.4854G=	XP_005267126.2:p.Met1618=
XM_011535984.1:c.3933G=	XP_011534286.1:p.Met1311=
XM_011535985.1:c.3753G=	XP_011534287.1:p.Met1251=
XM_011535986.1:c.3513G=	XP_011534288.1:p.Met1171=
XM_011535987.1:c.3132G=	XP_011534289.1:p.Met1044=
XM_011535988.1:c.1995G=	XP_011534290.1:p.Met665=
NM_001346813.1:c.4854G=	NP_001333742.1:p.Met1618=
NM_001363725.1:c.2604G=	NP_001350654.1:p.Met868=
XM_011535984.2:c.5064G=	XP_011534286.2:p.Met1688=
XM_011535988.3:c.1995G=	XP_011534290.1:p.Met665=
XM_017011103.2:c.4965G=	XP_016866592.1:p.Met1655=
XM_017011104.1:c.4935G=	XP_016866593.1:p.Met1645=
XM_017011105.2:c.4905G=	XP_016866594.1:p.Met1635=
XM_017011106.2:c.4776G=	XP_016866595.1:p.Met1592=
XM_017011107.2:c.4755G=	XP_016866596.1:p.Met1585=
XR_002956289.1:n.5050G=
NM_001363725.2:c.2604G=	NP_001350654.1:p.Met868=
NM_001371656.1:c.4983G=	NP_001358585.1:p.Met1661=
NM_001374820.1:c.4983G=	NP_001361749.1:p.Met1661=
NM_001374828.1:c.5103G= MANE Select	NP_001361757.1:p.Met1701=
NM_017519.3:c.4944G=	NP_059989.3:p.Met1648=