Canonical Allele Identifier: CA366248209

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207179G>A , CM000668.2:g.157207179G>A	GRCh38
NC_000006.11:g.157528313G>A , CM000668.1:g.157528313G>A	GRCh37
NC_000006.10:g.157570005G>A	NCBI36
NG_032093.1:g.434250G>A
NG_032093.2:g.434250G>A
NG_066624.1:g.436154G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.6248G>A	ENSP00000055163.8:p.Trp2083Ter
ENST00000414678.8:c.6317G>A	ENSP00000412835.3:p.Trp2106Ter
ENST00000637015.2:c.6536G>A	ENSP00000489729.2:p.Trp2179Ter
ENST00000346085.10:c.6287G>A	ENSP00000344546.5:p.Trp2096Ter
ENST00000350026.10:c.5999G>A	ENSP00000055163.7:p.Trp2000Ter
ENST00000414678.7:c.4565G>A	ENSP00000412835.2:p.Trp1522Ter
ENST00000635849.1:c.3728G>A	ENSP00000490948.1:p.Trp1243Ter
ENST00000635928.1:c.563G>A	ENSP00000489717.1:p.Trp188Ter
ENST00000635957.1:c.3359G>A	ENSP00000490385.1:p.Trp1120Ter
ENST00000636227.1:n.4870G>A
ENST00000636254.1:n.2327G>A
ENST00000636930.2:c.6407G>A MANE Select	ENSP00000490491.2:p.Trp2136Ter
ENST00000636940.1:n.4404G>A
ENST00000637015.1:c.3775G>A
ENST00000637568.1:c.3689G>A
ENST00000637741.1:n.3073G>A
ENST00000637810.1:c.3749G>A	ENSP00000489636.1:p.Trp1250Ter
ENST00000637904.1:c.3908G>A	ENSP00000490550.1:p.Trp1303Ter
ENST00000637933.1:n.3522G>A
ENST00000647938.1:c.6038G>A	ENSP00000498155.1:p.Trp2013Ter
ENST00000346085.9:c.6038G>A	ENSP00000344546.4:p.Trp2013Ter
ENST00000350026.9:c.5999G>A	ENSP00000055163.7:p.Trp2000Ter
ENST00000414678.6:c.4565G>A	ENSP00000412835.2:p.Trp1522Ter
NM_017519.2:c.5999G>A	NP_059989.2:p.Trp2000Ter
NM_020732.3:c.6038G>A	NP_065783.3:p.Trp2013Ter
XM_005267069.3:c.6158G>A	XP_005267126.2:p.Trp2053Ter
XM_011535984.1:c.5237G>A	XP_011534286.1:p.Trp1746Ter
XM_011535985.1:c.5057G>A	XP_011534287.1:p.Trp1686Ter
XM_011535986.1:c.4817G>A	XP_011534288.1:p.Trp1606Ter
XM_011535987.1:c.4436G>A	XP_011534289.1:p.Trp1479Ter
XM_011535988.1:c.3299G>A	XP_011534290.1:p.Trp1100Ter
NM_001346813.1:c.6158G>A	NP_001333742.1:p.Trp2053Ter
NM_001363725.1:c.3908G>A	NP_001350654.1:p.Trp1303Ter
XM_011535984.2:c.6368G>A	XP_011534286.2:p.Trp2123Ter
XM_011535988.3:c.3299G>A	XP_011534290.1:p.Trp1100Ter
XM_017011103.2:c.6269G>A	XP_016866592.1:p.Trp2090Ter
XM_017011104.1:c.6239G>A	XP_016866593.1:p.Trp2080Ter
XM_017011105.2:c.6209G>A	XP_016866594.1:p.Trp2070Ter
XM_017011106.2:c.6080G>A	XP_016866595.1:p.Trp2027Ter
XM_017011107.2:c.6059G>A	XP_016866596.1:p.Trp2020Ter
XR_002956289.1:n.6354G>A
NM_001363725.2:c.3908G>A	NP_001350654.1:p.Trp1303Ter
NM_001371656.1:c.6287G>A	NP_001358585.1:p.Trp2096Ter
NM_001374820.1:c.6287G>A	NP_001361749.1:p.Trp2096Ter
NM_001374828.1:c.6407G>A MANE Select	NP_001361757.1:p.Trp2136Ter
NM_017519.3:c.6248G>A	NP_059989.3:p.Trp2083Ter