Canonical Allele Identifier: CA366234213

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510881C>G (hg19) ; chr6:g.157189747C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189747C>G , CM000668.2:g.157189747C>G	GRCh38
NC_000006.11:g.157510881C>G , CM000668.1:g.157510881C>G	GRCh37
NC_000006.10:g.157552573C>G	NCBI36
NG_032093.1:g.416818C>G
NG_032093.2:g.416818C>G
NG_066624.1:g.418722C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3866C>G	ENSP00000055163.8:p.Pro1289Arg
ENST00000414678.8:c.3935C>G	ENSP00000412835.3:p.Pro1312Arg
ENST00000637015.2:c.4154C>G	ENSP00000489729.2:p.Pro1385Arg
ENST00000346085.10:c.3905C>G	ENSP00000344546.5:p.Pro1302Arg
ENST00000350026.10:c.3617C>G	ENSP00000055163.7:p.Pro1206Arg
ENST00000414678.7:c.2183C>G	ENSP00000412835.2:p.Pro728Arg
ENST00000635849.1:c.1346C>G	ENSP00000490948.1:p.Pro449Arg
ENST00000635957.1:c.980C>G	ENSP00000490385.1:p.Pro327Arg
ENST00000636930.2:c.4025C>G MANE Select	ENSP00000490491.2:p.Pro1342Arg
ENST00000636940.1:n.2022C>G
ENST00000637015.1:c.1393C>G
ENST00000637568.1:c.1307C>G
ENST00000637741.1:n.691C>G
ENST00000637810.1:c.1367C>G	ENSP00000489636.1:p.Pro456Arg
ENST00000637904.1:c.1526C>G	ENSP00000490550.1:p.Pro509Arg
ENST00000647938.1:c.3656C>G	ENSP00000498155.1:p.Pro1219Arg
ENST00000346085.9:c.3656C>G	ENSP00000344546.4:p.Pro1219Arg
ENST00000350026.9:c.3617C>G	ENSP00000055163.7:p.Pro1206Arg
ENST00000414678.6:c.2183C>G	ENSP00000412835.2:p.Pro728Arg
NM_017519.2:c.3617C>G	NP_059989.2:p.Pro1206Arg
NM_020732.3:c.3656C>G	NP_065783.3:p.Pro1219Arg
XM_005267069.3:c.3776C>G	XP_005267126.2:p.Pro1259Arg
XM_011535984.1:c.2855C>G	XP_011534286.1:p.Pro952Arg
XM_011535985.1:c.2675C>G	XP_011534287.1:p.Pro892Arg
XM_011535986.1:c.2435C>G	XP_011534288.1:p.Pro812Arg
XM_011535987.1:c.2054C>G	XP_011534289.1:p.Pro685Arg
XM_011535988.1:c.917C>G	XP_011534290.1:p.Pro306Arg
NM_001346813.1:c.3776C>G	NP_001333742.1:p.Pro1259Arg
NM_001363725.1:c.1526C>G	NP_001350654.1:p.Pro509Arg
XM_011535984.2:c.3986C>G	XP_011534286.2:p.Pro1329Arg
XM_011535988.3:c.917C>G	XP_011534290.1:p.Pro306Arg
XM_017011103.2:c.3887C>G	XP_016866592.1:p.Pro1296Arg
XM_017011104.1:c.3857C>G	XP_016866593.1:p.Pro1286Arg
XM_017011105.2:c.3827C>G	XP_016866594.1:p.Pro1276Arg
XM_017011106.2:c.3698C>G	XP_016866595.1:p.Pro1233Arg
XM_017011107.2:c.3677C>G	XP_016866596.1:p.Pro1226Arg
XR_002956289.1:n.4069C>G
NM_001363725.2:c.1526C>G	NP_001350654.1:p.Pro509Arg
NM_001371656.1:c.3905C>G	NP_001358585.1:p.Pro1302Arg
NM_001374820.1:c.3905C>G	NP_001361749.1:p.Pro1302Arg
NM_001374828.1:c.4025C>G MANE Select	NP_001361757.1:p.Pro1342Arg
NM_017519.3:c.3866C>G	NP_059989.3:p.Pro1289Arg