Canonical Allele Identifier: CA1675538273

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189770C= , CM000668.2:g.157189770C=	GRCh38
NC_000006.11:g.157510904C= , CM000668.1:g.157510904C=	GRCh37
NC_000006.10:g.157552596C=	NCBI36
NG_032093.1:g.416841C=
NG_032093.2:g.416841C=
NG_066624.1:g.418745C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3889C=	ENSP00000055163.8:p.Gln1297=
ENST00000414678.8:c.3958C=	ENSP00000412835.3:p.Gln1320=
ENST00000637015.2:c.4177C=	ENSP00000489729.2:p.Gln1393=
ENST00000346085.10:c.3928C=	ENSP00000344546.5:p.Gln1310=
ENST00000350026.10:c.3640C=	ENSP00000055163.7:p.Gln1214=
ENST00000414678.7:c.2206C=	ENSP00000412835.2:p.Gln736=
ENST00000635849.1:c.1369C=	ENSP00000490948.1:p.Gln457=
ENST00000635957.1:c.1003C=	ENSP00000490385.1:p.Gln335=
ENST00000636930.2:c.4048C= MANE Select	ENSP00000490491.2:p.Gln1350=
ENST00000636940.1:n.2045C=
ENST00000637015.1:c.1416C=
ENST00000637568.1:c.1330C=
ENST00000637741.1:n.714C=
ENST00000637810.1:c.1390C=	ENSP00000489636.1:p.Gln464=
ENST00000637904.1:c.1549C=	ENSP00000490550.1:p.Gln517=
ENST00000647938.1:c.3679C=	ENSP00000498155.1:p.Gln1227=
ENST00000346085.9:c.3679C=	ENSP00000344546.4:p.Gln1227=
ENST00000350026.9:c.3640C=	ENSP00000055163.7:p.Gln1214=
ENST00000414678.6:c.2206C=	ENSP00000412835.2:p.Gln736=
NM_017519.2:c.3640C=	NP_059989.2:p.Gln1214=
NM_020732.3:c.3679C=	NP_065783.3:p.Gln1227=
XM_005267069.3:c.3799C=	XP_005267126.2:p.Gln1267=
XM_011535984.1:c.2878C=	XP_011534286.1:p.Gln960=
XM_011535985.1:c.2698C=	XP_011534287.1:p.Gln900=
XM_011535986.1:c.2458C=	XP_011534288.1:p.Gln820=
XM_011535987.1:c.2077C=	XP_011534289.1:p.Gln693=
XM_011535988.1:c.940C=	XP_011534290.1:p.Gln314=
NM_001346813.1:c.3799C=	NP_001333742.1:p.Gln1267=
NM_001363725.1:c.1549C=	NP_001350654.1:p.Gln517=
XM_011535984.2:c.4009C=	XP_011534286.2:p.Gln1337=
XM_011535988.3:c.940C=	XP_011534290.1:p.Gln314=
XM_017011103.2:c.3910C=	XP_016866592.1:p.Gln1304=
XM_017011104.1:c.3880C=	XP_016866593.1:p.Gln1294=
XM_017011105.2:c.3850C=	XP_016866594.1:p.Gln1284=
XM_017011106.2:c.3721C=	XP_016866595.1:p.Gln1241=
XM_017011107.2:c.3700C=	XP_016866596.1:p.Gln1234=
XR_002956289.1:n.4092C=
NM_001363725.2:c.1549C=	NP_001350654.1:p.Gln517=
NM_001371656.1:c.3928C=	NP_001358585.1:p.Gln1310=
NM_001374820.1:c.3928C=	NP_001361749.1:p.Gln1310=
NM_001374828.1:c.4048C= MANE Select	NP_001361757.1:p.Gln1350=
NM_017519.3:c.3889C=	NP_059989.3:p.Gln1297=