Canonical Allele Identifier: CA366234212

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3866C>A	ENSP00000055163.8:p.Pro1289His
ENST00000414678.8:c.3935C>A	ENSP00000412835.3:p.Pro1312His
ENST00000637015.2:c.4154C>A	ENSP00000489729.2:p.Pro1385His
ENST00000346085.10:c.3905C>A	ENSP00000344546.5:p.Pro1302His
ENST00000350026.10:c.3617C>A	ENSP00000055163.7:p.Pro1206His
ENST00000414678.7:c.2183C>A	ENSP00000412835.2:p.Pro728His
ENST00000635849.1:c.1346C>A	ENSP00000490948.1:p.Pro449His
ENST00000635957.1:c.980C>A	ENSP00000490385.1:p.Pro327His
ENST00000636930.2:c.4025C>A MANE Select	ENSP00000490491.2:p.Pro1342His
ENST00000636940.1:n.2022C>A
ENST00000637015.1:c.1393C>A
ENST00000637568.1:c.1307C>A
ENST00000637741.1:n.691C>A
ENST00000637810.1:c.1367C>A	ENSP00000489636.1:p.Pro456His
ENST00000637904.1:c.1526C>A	ENSP00000490550.1:p.Pro509His
ENST00000647938.1:c.3656C>A	ENSP00000498155.1:p.Pro1219His
ENST00000346085.9:c.3656C>A	ENSP00000344546.4:p.Pro1219His
ENST00000350026.9:c.3617C>A	ENSP00000055163.7:p.Pro1206His
ENST00000414678.6:c.2183C>A	ENSP00000412835.2:p.Pro728His
NM_017519.2:c.3617C>A	NP_059989.2:p.Pro1206His
NM_020732.3:c.3656C>A	NP_065783.3:p.Pro1219His
XM_005267069.3:c.3776C>A	XP_005267126.2:p.Pro1259His
XM_011535984.1:c.2855C>A	XP_011534286.1:p.Pro952His
XM_011535985.1:c.2675C>A	XP_011534287.1:p.Pro892His
XM_011535986.1:c.2435C>A	XP_011534288.1:p.Pro812His
XM_011535987.1:c.2054C>A	XP_011534289.1:p.Pro685His
XM_011535988.1:c.917C>A	XP_011534290.1:p.Pro306His
NM_001346813.1:c.3776C>A	NP_001333742.1:p.Pro1259His
NM_001363725.1:c.1526C>A	NP_001350654.1:p.Pro509His
XM_011535984.2:c.3986C>A	XP_011534286.2:p.Pro1329His
XM_011535988.3:c.917C>A	XP_011534290.1:p.Pro306His
XM_017011103.2:c.3887C>A	XP_016866592.1:p.Pro1296His
XM_017011104.1:c.3857C>A	XP_016866593.1:p.Pro1286His
XM_017011105.2:c.3827C>A	XP_016866594.1:p.Pro1276His
XM_017011106.2:c.3698C>A	XP_016866595.1:p.Pro1233His
XM_017011107.2:c.3677C>A	XP_016866596.1:p.Pro1226His
XR_002956289.1:n.4069C>A
NM_001363725.2:c.1526C>A	NP_001350654.1:p.Pro509His
NM_001371656.1:c.3905C>A	NP_001358585.1:p.Pro1302His
NM_001374820.1:c.3905C>A	NP_001361749.1:p.Pro1302His
NM_001374828.1:c.4025C>A MANE Select	NP_001361757.1:p.Pro1342His
NM_017519.3:c.3866C>A	NP_059989.3:p.Pro1289His