Canonical Allele Identifier: CA366234219

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3869A>T	ENSP00000055163.8:p.His1290Leu
ENST00000414678.8:c.3938A>T	ENSP00000412835.3:p.His1313Leu
ENST00000637015.2:c.4157A>T	ENSP00000489729.2:p.His1386Leu
ENST00000346085.10:c.3908A>T	ENSP00000344546.5:p.His1303Leu
ENST00000350026.10:c.3620A>T	ENSP00000055163.7:p.His1207Leu
ENST00000414678.7:c.2186A>T	ENSP00000412835.2:p.His729Leu
ENST00000635849.1:c.1349A>T	ENSP00000490948.1:p.His450Leu
ENST00000635957.1:c.983A>T	ENSP00000490385.1:p.His328Leu
ENST00000636930.2:c.4028A>T MANE Select	ENSP00000490491.2:p.His1343Leu
ENST00000636940.1:n.2025A>T
ENST00000637015.1:c.1396A>T
ENST00000637568.1:c.1310A>T
ENST00000637741.1:n.694A>T
ENST00000637810.1:c.1370A>T	ENSP00000489636.1:p.His457Leu
ENST00000637904.1:c.1529A>T	ENSP00000490550.1:p.His510Leu
ENST00000647938.1:c.3659A>T	ENSP00000498155.1:p.His1220Leu
ENST00000346085.9:c.3659A>T	ENSP00000344546.4:p.His1220Leu
ENST00000350026.9:c.3620A>T	ENSP00000055163.7:p.His1207Leu
ENST00000414678.6:c.2186A>T	ENSP00000412835.2:p.His729Leu
NM_017519.2:c.3620A>T	NP_059989.2:p.His1207Leu
NM_020732.3:c.3659A>T	NP_065783.3:p.His1220Leu
XM_005267069.3:c.3779A>T	XP_005267126.2:p.His1260Leu
XM_011535984.1:c.2858A>T	XP_011534286.1:p.His953Leu
XM_011535985.1:c.2678A>T	XP_011534287.1:p.His893Leu
XM_011535986.1:c.2438A>T	XP_011534288.1:p.His813Leu
XM_011535987.1:c.2057A>T	XP_011534289.1:p.His686Leu
XM_011535988.1:c.920A>T	XP_011534290.1:p.His307Leu
NM_001346813.1:c.3779A>T	NP_001333742.1:p.His1260Leu
NM_001363725.1:c.1529A>T	NP_001350654.1:p.His510Leu
XM_011535984.2:c.3989A>T	XP_011534286.2:p.His1330Leu
XM_011535988.3:c.920A>T	XP_011534290.1:p.His307Leu
XM_017011103.2:c.3890A>T	XP_016866592.1:p.His1297Leu
XM_017011104.1:c.3860A>T	XP_016866593.1:p.His1287Leu
XM_017011105.2:c.3830A>T	XP_016866594.1:p.His1277Leu
XM_017011106.2:c.3701A>T	XP_016866595.1:p.His1234Leu
XM_017011107.2:c.3680A>T	XP_016866596.1:p.His1227Leu
XR_002956289.1:n.4072A>T
NM_001363725.2:c.1529A>T	NP_001350654.1:p.His510Leu
NM_001371656.1:c.3908A>T	NP_001358585.1:p.His1303Leu
NM_001374820.1:c.3908A>T	NP_001361749.1:p.His1303Leu
NM_001374828.1:c.4028A>T MANE Select	NP_001361757.1:p.His1343Leu
NM_017519.3:c.3869A>T	NP_059989.3:p.His1290Leu