Canonical Allele Identifier: CA1675538270

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189762C= , CM000668.2:g.157189762C=	GRCh38
NC_000006.11:g.157510896C= , CM000668.1:g.157510896C=	GRCh37
NC_000006.10:g.157552588C=	NCBI36
NG_032093.1:g.416833C=
NG_032093.2:g.416833C=
NG_066624.1:g.418737C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3881C=	ENSP00000055163.8:p.Thr1294=
ENST00000414678.8:c.3950C=	ENSP00000412835.3:p.Thr1317=
ENST00000637015.2:c.4169C=	ENSP00000489729.2:p.Thr1390=
ENST00000346085.10:c.3920C=	ENSP00000344546.5:p.Thr1307=
ENST00000350026.10:c.3632C=	ENSP00000055163.7:p.Thr1211=
ENST00000414678.7:c.2198C=	ENSP00000412835.2:p.Thr733=
ENST00000635849.1:c.1361C=	ENSP00000490948.1:p.Thr454=
ENST00000635957.1:c.995C=	ENSP00000490385.1:p.Thr332=
ENST00000636930.2:c.4040C= MANE Select	ENSP00000490491.2:p.Thr1347=
ENST00000636940.1:n.2037C=
ENST00000637015.1:c.1408C=
ENST00000637568.1:c.1322C=
ENST00000637741.1:n.706C=
ENST00000637810.1:c.1382C=	ENSP00000489636.1:p.Thr461=
ENST00000637904.1:c.1541C=	ENSP00000490550.1:p.Thr514=
ENST00000647938.1:c.3671C=	ENSP00000498155.1:p.Thr1224=
ENST00000346085.9:c.3671C=	ENSP00000344546.4:p.Thr1224=
ENST00000350026.9:c.3632C=	ENSP00000055163.7:p.Thr1211=
ENST00000414678.6:c.2198C=	ENSP00000412835.2:p.Thr733=
NM_017519.2:c.3632C=	NP_059989.2:p.Thr1211=
NM_020732.3:c.3671C=	NP_065783.3:p.Thr1224=
XM_005267069.3:c.3791C=	XP_005267126.2:p.Thr1264=
XM_011535984.1:c.2870C=	XP_011534286.1:p.Thr957=
XM_011535985.1:c.2690C=	XP_011534287.1:p.Thr897=
XM_011535986.1:c.2450C=	XP_011534288.1:p.Thr817=
XM_011535987.1:c.2069C=	XP_011534289.1:p.Thr690=
XM_011535988.1:c.932C=	XP_011534290.1:p.Thr311=
NM_001346813.1:c.3791C=	NP_001333742.1:p.Thr1264=
NM_001363725.1:c.1541C=	NP_001350654.1:p.Thr514=
XM_011535984.2:c.4001C=	XP_011534286.2:p.Thr1334=
XM_011535988.3:c.932C=	XP_011534290.1:p.Thr311=
XM_017011103.2:c.3902C=	XP_016866592.1:p.Thr1301=
XM_017011104.1:c.3872C=	XP_016866593.1:p.Thr1291=
XM_017011105.2:c.3842C=	XP_016866594.1:p.Thr1281=
XM_017011106.2:c.3713C=	XP_016866595.1:p.Thr1238=
XM_017011107.2:c.3692C=	XP_016866596.1:p.Thr1231=
XR_002956289.1:n.4084C=
NM_001363725.2:c.1541C=	NP_001350654.1:p.Thr514=
NM_001371656.1:c.3920C=	NP_001358585.1:p.Thr1307=
NM_001374820.1:c.3920C=	NP_001361749.1:p.Thr1307=
NM_001374828.1:c.4040C= MANE Select	NP_001361757.1:p.Thr1347=
NM_017519.3:c.3881C=	NP_059989.3:p.Thr1294=