Canonical Allele Identifier: CA1675538275

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189772A= , CM000668.2:g.157189772A=	GRCh38
NC_000006.11:g.157510906A= , CM000668.1:g.157510906A=	GRCh37
NC_000006.10:g.157552598A=	NCBI36
NG_032093.1:g.416843A=
NG_032093.2:g.416843A=
NG_066624.1:g.418747A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3891A=	ENSP00000055163.8:p.Gln1297=
ENST00000414678.8:c.3960A=	ENSP00000412835.3:p.Gln1320=
ENST00000637015.2:c.4179A=	ENSP00000489729.2:p.Gln1393=
ENST00000346085.10:c.3930A=	ENSP00000344546.5:p.Gln1310=
ENST00000350026.10:c.3642A=	ENSP00000055163.7:p.Gln1214=
ENST00000414678.7:c.2208A=	ENSP00000412835.2:p.Gln736=
ENST00000635849.1:c.1371A=	ENSP00000490948.1:p.Gln457=
ENST00000635957.1:c.1005A=	ENSP00000490385.1:p.Gln335=
ENST00000636930.2:c.4050A= MANE Select	ENSP00000490491.2:p.Gln1350=
ENST00000636940.1:n.2047A=
ENST00000637015.1:c.1418A=
ENST00000637568.1:c.1332A=
ENST00000637741.1:n.716A=
ENST00000637810.1:c.1392A=	ENSP00000489636.1:p.Gln464=
ENST00000637904.1:c.1551A=	ENSP00000490550.1:p.Gln517=
ENST00000647938.1:c.3681A=	ENSP00000498155.1:p.Gln1227=
ENST00000346085.9:c.3681A=	ENSP00000344546.4:p.Gln1227=
ENST00000350026.9:c.3642A=	ENSP00000055163.7:p.Gln1214=
ENST00000414678.6:c.2208A=	ENSP00000412835.2:p.Gln736=
NM_017519.2:c.3642A=	NP_059989.2:p.Gln1214=
NM_020732.3:c.3681A=	NP_065783.3:p.Gln1227=
XM_005267069.3:c.3801A=	XP_005267126.2:p.Gln1267=
XM_011535984.1:c.2880A=	XP_011534286.1:p.Gln960=
XM_011535985.1:c.2700A=	XP_011534287.1:p.Gln900=
XM_011535986.1:c.2460A=	XP_011534288.1:p.Gln820=
XM_011535987.1:c.2079A=	XP_011534289.1:p.Gln693=
XM_011535988.1:c.942A=	XP_011534290.1:p.Gln314=
NM_001346813.1:c.3801A=	NP_001333742.1:p.Gln1267=
NM_001363725.1:c.1551A=	NP_001350654.1:p.Gln517=
XM_011535984.2:c.4011A=	XP_011534286.2:p.Gln1337=
XM_011535988.3:c.942A=	XP_011534290.1:p.Gln314=
XM_017011103.2:c.3912A=	XP_016866592.1:p.Gln1304=
XM_017011104.1:c.3882A=	XP_016866593.1:p.Gln1294=
XM_017011105.2:c.3852A=	XP_016866594.1:p.Gln1284=
XM_017011106.2:c.3723A=	XP_016866595.1:p.Gln1241=
XM_017011107.2:c.3702A=	XP_016866596.1:p.Gln1234=
XR_002956289.1:n.4094A=
NM_001363725.2:c.1551A=	NP_001350654.1:p.Gln517=
NM_001371656.1:c.3930A=	NP_001358585.1:p.Gln1310=
NM_001374820.1:c.3930A=	NP_001361749.1:p.Gln1310=
NM_001374828.1:c.4050A= MANE Select	NP_001361757.1:p.Gln1350=
NM_017519.3:c.3891A=	NP_059989.3:p.Gln1297=