Canonical Allele Identifier: CA366239436

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157519946C>G (hg19) ; chr6:g.157198812C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198812C>G , CM000668.2:g.157198812C>G	GRCh38
NC_000006.11:g.157519946C>G , CM000668.1:g.157519946C>G	GRCh37
NC_000006.10:g.157561638C>G	NCBI36
NG_032093.1:g.425883C>G
NG_032093.2:g.425883C>G
NG_066624.1:g.427787C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4225C>G	ENSP00000055163.8:p.His1409Asp
ENST00000414678.8:c.4294C>G	ENSP00000412835.3:p.His1432Asp
ENST00000637015.2:c.4513C>G	ENSP00000489729.2:p.His1505Asp
ENST00000346085.10:c.4264C>G	ENSP00000344546.5:p.His1422Asp
ENST00000350026.10:c.3976C>G	ENSP00000055163.7:p.His1326Asp
ENST00000414678.7:c.2542C>G	ENSP00000412835.2:p.His848Asp
ENST00000635849.1:c.1705C>G	ENSP00000490948.1:p.His569Asp
ENST00000635957.1:c.1336C>G	ENSP00000490385.1:p.His446Asp
ENST00000636227.1:n.2847C>G
ENST00000636254.1:n.304C>G
ENST00000636930.2:c.4384C>G MANE Select	ENSP00000490491.2:p.His1462Asp
ENST00000636940.1:n.2381C>G
ENST00000637015.1:c.1752C>G
ENST00000637568.1:c.1666C>G
ENST00000637741.1:n.1050C>G
ENST00000637810.1:c.1726C>G	ENSP00000489636.1:p.His576Asp
ENST00000637904.1:c.1885C>G	ENSP00000490550.1:p.His629Asp
ENST00000647938.1:c.4015C>G	ENSP00000498155.1:p.His1339Asp
ENST00000346085.9:c.4015C>G	ENSP00000344546.4:p.His1339Asp
ENST00000350026.9:c.3976C>G	ENSP00000055163.7:p.His1326Asp
ENST00000414678.6:c.2542C>G	ENSP00000412835.2:p.His848Asp
NM_017519.2:c.3976C>G	NP_059989.2:p.His1326Asp
NM_020732.3:c.4015C>G	NP_065783.3:p.His1339Asp
XM_005267069.3:c.4135C>G	XP_005267126.2:p.His1379Asp
XM_011535984.1:c.3214C>G	XP_011534286.1:p.His1072Asp
XM_011535985.1:c.3034C>G	XP_011534287.1:p.His1012Asp
XM_011535986.1:c.2794C>G	XP_011534288.1:p.His932Asp
XM_011535987.1:c.2413C>G	XP_011534289.1:p.His805Asp
XM_011535988.1:c.1276C>G	XP_011534290.1:p.His426Asp
NM_001346813.1:c.4135C>G	NP_001333742.1:p.His1379Asp
NM_001363725.1:c.1885C>G	NP_001350654.1:p.His629Asp
XM_011535984.2:c.4345C>G	XP_011534286.2:p.His1449Asp
XM_011535988.3:c.1276C>G	XP_011534290.1:p.His426Asp
XM_017011103.2:c.4246C>G	XP_016866592.1:p.His1416Asp
XM_017011104.1:c.4216C>G	XP_016866593.1:p.His1406Asp
XM_017011105.2:c.4186C>G	XP_016866594.1:p.His1396Asp
XM_017011106.2:c.4057C>G	XP_016866595.1:p.His1353Asp
XM_017011107.2:c.4036C>G	XP_016866596.1:p.His1346Asp
XR_002956289.1:n.4427-1893C>G
NM_001363725.2:c.1885C>G	NP_001350654.1:p.His629Asp
NM_001371656.1:c.4264C>G	NP_001358585.1:p.His1422Asp
NM_001374820.1:c.4264C>G	NP_001361749.1:p.His1422Asp
NM_001374828.1:c.4384C>G MANE Select	NP_001361757.1:p.His1462Asp
NM_017519.3:c.4225C>G	NP_059989.3:p.His1409Asp