Canonical Allele Identifier: CA366234217

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510883C>T (hg19) ; chr6:g.157189749C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189749C>T , CM000668.2:g.157189749C>T	GRCh38
NC_000006.11:g.157510883C>T , CM000668.1:g.157510883C>T	GRCh37
NC_000006.10:g.157552575C>T	NCBI36
NG_032093.1:g.416820C>T
NG_032093.2:g.416820C>T
NG_066624.1:g.418724C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3868C>T	ENSP00000055163.8:p.His1290Tyr
ENST00000414678.8:c.3937C>T	ENSP00000412835.3:p.His1313Tyr
ENST00000637015.2:c.4156C>T	ENSP00000489729.2:p.His1386Tyr
ENST00000346085.10:c.3907C>T	ENSP00000344546.5:p.His1303Tyr
ENST00000350026.10:c.3619C>T	ENSP00000055163.7:p.His1207Tyr
ENST00000414678.7:c.2185C>T	ENSP00000412835.2:p.His729Tyr
ENST00000635849.1:c.1348C>T	ENSP00000490948.1:p.His450Tyr
ENST00000635957.1:c.982C>T	ENSP00000490385.1:p.His328Tyr
ENST00000636930.2:c.4027C>T MANE Select	ENSP00000490491.2:p.His1343Tyr
ENST00000636940.1:n.2024C>T
ENST00000637015.1:c.1395C>T
ENST00000637568.1:c.1309C>T
ENST00000637741.1:n.693C>T
ENST00000637810.1:c.1369C>T	ENSP00000489636.1:p.His457Tyr
ENST00000637904.1:c.1528C>T	ENSP00000490550.1:p.His510Tyr
ENST00000647938.1:c.3658C>T	ENSP00000498155.1:p.His1220Tyr
ENST00000346085.9:c.3658C>T	ENSP00000344546.4:p.His1220Tyr
ENST00000350026.9:c.3619C>T	ENSP00000055163.7:p.His1207Tyr
ENST00000414678.6:c.2185C>T	ENSP00000412835.2:p.His729Tyr
NM_017519.2:c.3619C>T	NP_059989.2:p.His1207Tyr
NM_020732.3:c.3658C>T	NP_065783.3:p.His1220Tyr
XM_005267069.3:c.3778C>T	XP_005267126.2:p.His1260Tyr
XM_011535984.1:c.2857C>T	XP_011534286.1:p.His953Tyr
XM_011535985.1:c.2677C>T	XP_011534287.1:p.His893Tyr
XM_011535986.1:c.2437C>T	XP_011534288.1:p.His813Tyr
XM_011535987.1:c.2056C>T	XP_011534289.1:p.His686Tyr
XM_011535988.1:c.919C>T	XP_011534290.1:p.His307Tyr
NM_001346813.1:c.3778C>T	NP_001333742.1:p.His1260Tyr
NM_001363725.1:c.1528C>T	NP_001350654.1:p.His510Tyr
XM_011535984.2:c.3988C>T	XP_011534286.2:p.His1330Tyr
XM_011535988.3:c.919C>T	XP_011534290.1:p.His307Tyr
XM_017011103.2:c.3889C>T	XP_016866592.1:p.His1297Tyr
XM_017011104.1:c.3859C>T	XP_016866593.1:p.His1287Tyr
XM_017011105.2:c.3829C>T	XP_016866594.1:p.His1277Tyr
XM_017011106.2:c.3700C>T	XP_016866595.1:p.His1234Tyr
XM_017011107.2:c.3679C>T	XP_016866596.1:p.His1227Tyr
XR_002956289.1:n.4071C>T
NM_001363725.2:c.1528C>T	NP_001350654.1:p.His510Tyr
NM_001371656.1:c.3907C>T	NP_001358585.1:p.His1303Tyr
NM_001374820.1:c.3907C>T	NP_001361749.1:p.His1303Tyr
NM_001374828.1:c.4027C>T MANE Select	NP_001361757.1:p.His1343Tyr
NM_017519.3:c.3868C>T	NP_059989.3:p.His1290Tyr