Canonical Allele Identifier: CA366234216

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3868C>G	ENSP00000055163.8:p.His1290Asp
ENST00000414678.8:c.3937C>G	ENSP00000412835.3:p.His1313Asp
ENST00000637015.2:c.4156C>G	ENSP00000489729.2:p.His1386Asp
ENST00000346085.10:c.3907C>G	ENSP00000344546.5:p.His1303Asp
ENST00000350026.10:c.3619C>G	ENSP00000055163.7:p.His1207Asp
ENST00000414678.7:c.2185C>G	ENSP00000412835.2:p.His729Asp
ENST00000635849.1:c.1348C>G	ENSP00000490948.1:p.His450Asp
ENST00000635957.1:c.982C>G	ENSP00000490385.1:p.His328Asp
ENST00000636930.2:c.4027C>G MANE Select	ENSP00000490491.2:p.His1343Asp
ENST00000636940.1:n.2024C>G
ENST00000637015.1:c.1395C>G
ENST00000637568.1:c.1309C>G
ENST00000637741.1:n.693C>G
ENST00000637810.1:c.1369C>G	ENSP00000489636.1:p.His457Asp
ENST00000637904.1:c.1528C>G	ENSP00000490550.1:p.His510Asp
ENST00000647938.1:c.3658C>G	ENSP00000498155.1:p.His1220Asp
ENST00000346085.9:c.3658C>G	ENSP00000344546.4:p.His1220Asp
ENST00000350026.9:c.3619C>G	ENSP00000055163.7:p.His1207Asp
ENST00000414678.6:c.2185C>G	ENSP00000412835.2:p.His729Asp
NM_017519.2:c.3619C>G	NP_059989.2:p.His1207Asp
NM_020732.3:c.3658C>G	NP_065783.3:p.His1220Asp
XM_005267069.3:c.3778C>G	XP_005267126.2:p.His1260Asp
XM_011535984.1:c.2857C>G	XP_011534286.1:p.His953Asp
XM_011535985.1:c.2677C>G	XP_011534287.1:p.His893Asp
XM_011535986.1:c.2437C>G	XP_011534288.1:p.His813Asp
XM_011535987.1:c.2056C>G	XP_011534289.1:p.His686Asp
XM_011535988.1:c.919C>G	XP_011534290.1:p.His307Asp
NM_001346813.1:c.3778C>G	NP_001333742.1:p.His1260Asp
NM_001363725.1:c.1528C>G	NP_001350654.1:p.His510Asp
XM_011535984.2:c.3988C>G	XP_011534286.2:p.His1330Asp
XM_011535988.3:c.919C>G	XP_011534290.1:p.His307Asp
XM_017011103.2:c.3889C>G	XP_016866592.1:p.His1297Asp
XM_017011104.1:c.3859C>G	XP_016866593.1:p.His1287Asp
XM_017011105.2:c.3829C>G	XP_016866594.1:p.His1277Asp
XM_017011106.2:c.3700C>G	XP_016866595.1:p.His1234Asp
XM_017011107.2:c.3679C>G	XP_016866596.1:p.His1227Asp
XR_002956289.1:n.4071C>G
NM_001363725.2:c.1528C>G	NP_001350654.1:p.His510Asp
NM_001371656.1:c.3907C>G	NP_001358585.1:p.His1303Asp
NM_001374820.1:c.3907C>G	NP_001361749.1:p.His1303Asp
NM_001374828.1:c.4027C>G MANE Select	NP_001361757.1:p.His1343Asp
NM_017519.3:c.3868C>G	NP_059989.3:p.His1290Asp