Canonical Allele Identifier: CA366233991

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510776C>A (hg19) ; chr6:g.157189642C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189642C>A , CM000668.2:g.157189642C>A	GRCh38
NC_000006.11:g.157510776C>A , CM000668.1:g.157510776C>A	GRCh37
NC_000006.10:g.157552468C>A	NCBI36
NG_032093.1:g.416713C>A
NG_032093.2:g.416713C>A
NG_066624.1:g.418617C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3761C>A	ENSP00000055163.8:p.Ala1254Asp
ENST00000414678.8:c.3830C>A	ENSP00000412835.3:p.Ala1277Asp
ENST00000637015.2:c.4049C>A	ENSP00000489729.2:p.Ala1350Asp
ENST00000346085.10:c.3800C>A	ENSP00000344546.5:p.Ala1267Asp
ENST00000350026.10:c.3512C>A	ENSP00000055163.7:p.Ala1171Asp
ENST00000414678.7:c.2078C>A	ENSP00000412835.2:p.Ala693Asp
ENST00000635849.1:c.1241C>A	ENSP00000490948.1:p.Ala414Asp
ENST00000635957.1:c.875C>A	ENSP00000490385.1:p.Ala292Asp
ENST00000636930.2:c.3920C>A MANE Select	ENSP00000490491.2:p.Ala1307Asp
ENST00000636940.1:n.1917C>A
ENST00000637015.1:c.1288C>A
ENST00000637568.1:c.1202C>A
ENST00000637741.1:n.586C>A
ENST00000637810.1:c.1262C>A	ENSP00000489636.1:p.Ala421Asp
ENST00000637904.1:c.1421C>A	ENSP00000490550.1:p.Ala474Asp
ENST00000647938.1:c.3551C>A	ENSP00000498155.1:p.Ala1184Asp
ENST00000346085.9:c.3551C>A	ENSP00000344546.4:p.Ala1184Asp
ENST00000350026.9:c.3512C>A	ENSP00000055163.7:p.Ala1171Asp
ENST00000414678.6:c.2078C>A	ENSP00000412835.2:p.Ala693Asp
NM_017519.2:c.3512C>A	NP_059989.2:p.Ala1171Asp
NM_020732.3:c.3551C>A	NP_065783.3:p.Ala1184Asp
XM_005267069.3:c.3671C>A	XP_005267126.2:p.Ala1224Asp
XM_011535984.1:c.2750C>A	XP_011534286.1:p.Ala917Asp
XM_011535985.1:c.2570C>A	XP_011534287.1:p.Ala857Asp
XM_011535986.1:c.2330C>A	XP_011534288.1:p.Ala777Asp
XM_011535987.1:c.1949C>A	XP_011534289.1:p.Ala650Asp
XM_011535988.1:c.812C>A	XP_011534290.1:p.Ala271Asp
NM_001346813.1:c.3671C>A	NP_001333742.1:p.Ala1224Asp
NM_001363725.1:c.1421C>A	NP_001350654.1:p.Ala474Asp
XM_011535984.2:c.3881C>A	XP_011534286.2:p.Ala1294Asp
XM_011535988.3:c.812C>A	XP_011534290.1:p.Ala271Asp
XM_017011103.2:c.3782C>A	XP_016866592.1:p.Ala1261Asp
XM_017011104.1:c.3752C>A	XP_016866593.1:p.Ala1251Asp
XM_017011105.2:c.3722C>A	XP_016866594.1:p.Ala1241Asp
XM_017011106.2:c.3593C>A	XP_016866595.1:p.Ala1198Asp
XM_017011107.2:c.3572C>A	XP_016866596.1:p.Ala1191Asp
XR_002956289.1:n.3964C>A
NM_001363725.2:c.1421C>A	NP_001350654.1:p.Ala474Asp
NM_001371656.1:c.3800C>A	NP_001358585.1:p.Ala1267Asp
NM_001374820.1:c.3800C>A	NP_001361749.1:p.Ala1267Asp
NM_001374828.1:c.3920C>A MANE Select	NP_001361757.1:p.Ala1307Asp
NM_017519.3:c.3761C>A	NP_059989.3:p.Ala1254Asp