Canonical Allele Identifier: CA366234220

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510884A>G (hg19) ; chr6:g.157189750A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189750A>G , CM000668.2:g.157189750A>G	GRCh38
NC_000006.11:g.157510884A>G , CM000668.1:g.157510884A>G	GRCh37
NC_000006.10:g.157552576A>G	NCBI36
NG_032093.1:g.416821A>G
NG_032093.2:g.416821A>G
NG_066624.1:g.418725A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3869A>G	ENSP00000055163.8:p.His1290Arg
ENST00000414678.8:c.3938A>G	ENSP00000412835.3:p.His1313Arg
ENST00000637015.2:c.4157A>G	ENSP00000489729.2:p.His1386Arg
ENST00000346085.10:c.3908A>G	ENSP00000344546.5:p.His1303Arg
ENST00000350026.10:c.3620A>G	ENSP00000055163.7:p.His1207Arg
ENST00000414678.7:c.2186A>G	ENSP00000412835.2:p.His729Arg
ENST00000635849.1:c.1349A>G	ENSP00000490948.1:p.His450Arg
ENST00000635957.1:c.983A>G	ENSP00000490385.1:p.His328Arg
ENST00000636930.2:c.4028A>G MANE Select	ENSP00000490491.2:p.His1343Arg
ENST00000636940.1:n.2025A>G
ENST00000637015.1:c.1396A>G
ENST00000637568.1:c.1310A>G
ENST00000637741.1:n.694A>G
ENST00000637810.1:c.1370A>G	ENSP00000489636.1:p.His457Arg
ENST00000637904.1:c.1529A>G	ENSP00000490550.1:p.His510Arg
ENST00000647938.1:c.3659A>G	ENSP00000498155.1:p.His1220Arg
ENST00000346085.9:c.3659A>G	ENSP00000344546.4:p.His1220Arg
ENST00000350026.9:c.3620A>G	ENSP00000055163.7:p.His1207Arg
ENST00000414678.6:c.2186A>G	ENSP00000412835.2:p.His729Arg
NM_017519.2:c.3620A>G	NP_059989.2:p.His1207Arg
NM_020732.3:c.3659A>G	NP_065783.3:p.His1220Arg
XM_005267069.3:c.3779A>G	XP_005267126.2:p.His1260Arg
XM_011535984.1:c.2858A>G	XP_011534286.1:p.His953Arg
XM_011535985.1:c.2678A>G	XP_011534287.1:p.His893Arg
XM_011535986.1:c.2438A>G	XP_011534288.1:p.His813Arg
XM_011535987.1:c.2057A>G	XP_011534289.1:p.His686Arg
XM_011535988.1:c.920A>G	XP_011534290.1:p.His307Arg
NM_001346813.1:c.3779A>G	NP_001333742.1:p.His1260Arg
NM_001363725.1:c.1529A>G	NP_001350654.1:p.His510Arg
XM_011535984.2:c.3989A>G	XP_011534286.2:p.His1330Arg
XM_011535988.3:c.920A>G	XP_011534290.1:p.His307Arg
XM_017011103.2:c.3890A>G	XP_016866592.1:p.His1297Arg
XM_017011104.1:c.3860A>G	XP_016866593.1:p.His1287Arg
XM_017011105.2:c.3830A>G	XP_016866594.1:p.His1277Arg
XM_017011106.2:c.3701A>G	XP_016866595.1:p.His1234Arg
XM_017011107.2:c.3680A>G	XP_016866596.1:p.His1227Arg
XR_002956289.1:n.4072A>G
NM_001363725.2:c.1529A>G	NP_001350654.1:p.His510Arg
NM_001371656.1:c.3908A>G	NP_001358585.1:p.His1303Arg
NM_001374820.1:c.3908A>G	NP_001361749.1:p.His1303Arg
NM_001374828.1:c.4028A>G MANE Select	NP_001361757.1:p.His1343Arg
NM_017519.3:c.3869A>G	NP_059989.3:p.His1290Arg