Canonical Allele Identifier: CA366234183

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510866C>G (hg19) ; chr6:g.157189732C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189732C>G , CM000668.2:g.157189732C>G	GRCh38
NC_000006.11:g.157510866C>G , CM000668.1:g.157510866C>G	GRCh37
NC_000006.10:g.157552558C>G	NCBI36
NG_032093.1:g.416803C>G
NG_032093.2:g.416803C>G
NG_066624.1:g.418707C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3851C>G	ENSP00000055163.8:p.Thr1284Ser
ENST00000414678.8:c.3920C>G	ENSP00000412835.3:p.Thr1307Ser
ENST00000637015.2:c.4139C>G	ENSP00000489729.2:p.Thr1380Ser
ENST00000346085.10:c.3890C>G	ENSP00000344546.5:p.Thr1297Ser
ENST00000350026.10:c.3602C>G	ENSP00000055163.7:p.Thr1201Ser
ENST00000414678.7:c.2168C>G	ENSP00000412835.2:p.Thr723Ser
ENST00000635849.1:c.1331C>G	ENSP00000490948.1:p.Thr444Ser
ENST00000635957.1:c.965C>G	ENSP00000490385.1:p.Thr322Ser
ENST00000636930.2:c.4010C>G MANE Select	ENSP00000490491.2:p.Thr1337Ser
ENST00000636940.1:n.2007C>G
ENST00000637015.1:c.1378C>G
ENST00000637568.1:c.1292C>G
ENST00000637741.1:n.676C>G
ENST00000637810.1:c.1352C>G	ENSP00000489636.1:p.Thr451Ser
ENST00000637904.1:c.1511C>G	ENSP00000490550.1:p.Thr504Ser
ENST00000647938.1:c.3641C>G	ENSP00000498155.1:p.Thr1214Ser
ENST00000346085.9:c.3641C>G	ENSP00000344546.4:p.Thr1214Ser
ENST00000350026.9:c.3602C>G	ENSP00000055163.7:p.Thr1201Ser
ENST00000414678.6:c.2168C>G	ENSP00000412835.2:p.Thr723Ser
NM_017519.2:c.3602C>G	NP_059989.2:p.Thr1201Ser
NM_020732.3:c.3641C>G	NP_065783.3:p.Thr1214Ser
XM_005267069.3:c.3761C>G	XP_005267126.2:p.Thr1254Ser
XM_011535984.1:c.2840C>G	XP_011534286.1:p.Thr947Ser
XM_011535985.1:c.2660C>G	XP_011534287.1:p.Thr887Ser
XM_011535986.1:c.2420C>G	XP_011534288.1:p.Thr807Ser
XM_011535987.1:c.2039C>G	XP_011534289.1:p.Thr680Ser
XM_011535988.1:c.902C>G	XP_011534290.1:p.Thr301Ser
NM_001346813.1:c.3761C>G	NP_001333742.1:p.Thr1254Ser
NM_001363725.1:c.1511C>G	NP_001350654.1:p.Thr504Ser
XM_011535984.2:c.3971C>G	XP_011534286.2:p.Thr1324Ser
XM_011535988.3:c.902C>G	XP_011534290.1:p.Thr301Ser
XM_017011103.2:c.3872C>G	XP_016866592.1:p.Thr1291Ser
XM_017011104.1:c.3842C>G	XP_016866593.1:p.Thr1281Ser
XM_017011105.2:c.3812C>G	XP_016866594.1:p.Thr1271Ser
XM_017011106.2:c.3683C>G	XP_016866595.1:p.Thr1228Ser
XM_017011107.2:c.3662C>G	XP_016866596.1:p.Thr1221Ser
XR_002956289.1:n.4054C>G
NM_001363725.2:c.1511C>G	NP_001350654.1:p.Thr504Ser
NM_001371656.1:c.3890C>G	NP_001358585.1:p.Thr1297Ser
NM_001374820.1:c.3890C>G	NP_001361749.1:p.Thr1297Ser
NM_001374828.1:c.4010C>G MANE Select	NP_001361757.1:p.Thr1337Ser
NM_017519.3:c.3851C>G	NP_059989.3:p.Thr1284Ser