Canonical Allele Identifier: CA366238456

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157196248G>C , CM000668.2:g.157196248G>C	GRCh38
NC_000006.11:g.157517382G>C , CM000668.1:g.157517382G>C	GRCh37
NC_000006.10:g.157559074G>C	NCBI36
NG_032093.1:g.423319G>C
NG_032093.2:g.423319G>C
NG_066624.1:g.425223G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4315G>C MANE Select	NP_001361757.1:p.Gly1439Arg
ENST00000636930.2:c.4315G>C MANE Select	ENSP00000490491.2:p.Gly1439Arg
NM_001346813.1:c.4066G>C	NP_001333742.1:p.Gly1356Arg
NM_001363725.1:c.1816G>C	NP_001350654.1:p.Gly606Arg
NM_001363725.2:c.1816G>C	NP_001350654.1:p.Gly606Arg
NM_001371656.1:c.4195G>C	NP_001358585.1:p.Gly1399Arg
NM_001374820.1:c.4195G>C	NP_001361749.1:p.Gly1399Arg
NM_017519.2:c.3907G>C	NP_059989.2:p.Gly1303Arg
NM_017519.3:c.4156G>C	NP_059989.3:p.Gly1386Arg
NM_020732.3:c.3946G>C	NP_065783.3:p.Gly1316Arg
ENST00000346085.10:c.4195G>C	ENSP00000344546.5:p.Gly1399Arg
ENST00000346085.9:c.3946G>C	ENSP00000344546.4:p.Gly1316Arg
ENST00000350026.10:c.3907G>C	ENSP00000055163.7:p.Gly1303Arg
ENST00000350026.11:c.4156G>C	ENSP00000055163.8:p.Gly1386Arg
ENST00000350026.9:c.3907G>C	ENSP00000055163.7:p.Gly1303Arg
ENST00000414678.6:c.2473G>C	ENSP00000412835.2:p.Gly825Arg
ENST00000414678.7:c.2473G>C	ENSP00000412835.2:p.Gly825Arg
ENST00000414678.8:c.4225G>C	ENSP00000412835.3:p.Gly1409Arg
ENST00000635849.1:c.1636G>C	ENSP00000490948.1:p.Gly546Arg
ENST00000635957.1:c.1267G>C	ENSP00000490385.1:p.Gly423Arg
ENST00000636227.1:n.2778G>C
ENST00000636940.1:n.2312G>C
ENST00000637015.1:c.1683G>C
ENST00000637015.2:c.4444G>C	ENSP00000489729.2:p.Gly1482Arg
ENST00000637568.1:c.1597G>C
ENST00000637741.1:n.981G>C
ENST00000637810.1:c.1657G>C	ENSP00000489636.1:p.Gly553Arg
ENST00000637904.1:c.1816G>C	ENSP00000490550.1:p.Gly606Arg
ENST00000647938.1:c.3946G>C	ENSP00000498155.1:p.Gly1316Arg
XM_005267069.3:c.4066G>C	XP_005267126.2:p.Gly1356Arg
XM_011535984.1:c.3145G>C	XP_011534286.1:p.Gly1049Arg
XM_011535984.2:c.4276G>C	XP_011534286.2:p.Gly1426Arg
XM_011535985.1:c.2965G>C	XP_011534287.1:p.Gly989Arg
XM_011535986.1:c.2725G>C	XP_011534288.1:p.Gly909Arg
XM_011535987.1:c.2344G>C	XP_011534289.1:p.Gly782Arg
XM_011535988.1:c.1207G>C	XP_011534290.1:p.Gly403Arg
XM_011535988.3:c.1207G>C	XP_011534290.1:p.Gly403Arg
XM_017011103.2:c.4177G>C	XP_016866592.1:p.Gly1393Arg
XM_017011104.1:c.4147G>C	XP_016866593.1:p.Gly1383Arg
XM_017011105.2:c.4117G>C	XP_016866594.1:p.Gly1373Arg
XM_017011106.2:c.3988G>C	XP_016866595.1:p.Gly1330Arg
XM_017011107.2:c.3967G>C	XP_016866596.1:p.Gly1323Arg
XR_002956289.1:n.4359G>C