Canonical Allele Identifier: CA366234214

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3866C>T	ENSP00000055163.8:p.Pro1289Leu
ENST00000414678.8:c.3935C>T	ENSP00000412835.3:p.Pro1312Leu
ENST00000637015.2:c.4154C>T	ENSP00000489729.2:p.Pro1385Leu
ENST00000346085.10:c.3905C>T	ENSP00000344546.5:p.Pro1302Leu
ENST00000350026.10:c.3617C>T	ENSP00000055163.7:p.Pro1206Leu
ENST00000414678.7:c.2183C>T	ENSP00000412835.2:p.Pro728Leu
ENST00000635849.1:c.1346C>T	ENSP00000490948.1:p.Pro449Leu
ENST00000635957.1:c.980C>T	ENSP00000490385.1:p.Pro327Leu
ENST00000636930.2:c.4025C>T MANE Select	ENSP00000490491.2:p.Pro1342Leu
ENST00000636940.1:n.2022C>T
ENST00000637015.1:c.1393C>T
ENST00000637568.1:c.1307C>T
ENST00000637741.1:n.691C>T
ENST00000637810.1:c.1367C>T	ENSP00000489636.1:p.Pro456Leu
ENST00000637904.1:c.1526C>T	ENSP00000490550.1:p.Pro509Leu
ENST00000647938.1:c.3656C>T	ENSP00000498155.1:p.Pro1219Leu
ENST00000346085.9:c.3656C>T	ENSP00000344546.4:p.Pro1219Leu
ENST00000350026.9:c.3617C>T	ENSP00000055163.7:p.Pro1206Leu
ENST00000414678.6:c.2183C>T	ENSP00000412835.2:p.Pro728Leu
NM_017519.2:c.3617C>T	NP_059989.2:p.Pro1206Leu
NM_020732.3:c.3656C>T	NP_065783.3:p.Pro1219Leu
XM_005267069.3:c.3776C>T	XP_005267126.2:p.Pro1259Leu
XM_011535984.1:c.2855C>T	XP_011534286.1:p.Pro952Leu
XM_011535985.1:c.2675C>T	XP_011534287.1:p.Pro892Leu
XM_011535986.1:c.2435C>T	XP_011534288.1:p.Pro812Leu
XM_011535987.1:c.2054C>T	XP_011534289.1:p.Pro685Leu
XM_011535988.1:c.917C>T	XP_011534290.1:p.Pro306Leu
NM_001346813.1:c.3776C>T	NP_001333742.1:p.Pro1259Leu
NM_001363725.1:c.1526C>T	NP_001350654.1:p.Pro509Leu
XM_011535984.2:c.3986C>T	XP_011534286.2:p.Pro1329Leu
XM_011535988.3:c.917C>T	XP_011534290.1:p.Pro306Leu
XM_017011103.2:c.3887C>T	XP_016866592.1:p.Pro1296Leu
XM_017011104.1:c.3857C>T	XP_016866593.1:p.Pro1286Leu
XM_017011105.2:c.3827C>T	XP_016866594.1:p.Pro1276Leu
XM_017011106.2:c.3698C>T	XP_016866595.1:p.Pro1233Leu
XM_017011107.2:c.3677C>T	XP_016866596.1:p.Pro1226Leu
XR_002956289.1:n.4069C>T
NM_001363725.2:c.1526C>T	NP_001350654.1:p.Pro509Leu
NM_001371656.1:c.3905C>T	NP_001358585.1:p.Pro1302Leu
NM_001374820.1:c.3905C>T	NP_001361749.1:p.Pro1302Leu
NM_001374828.1:c.4025C>T MANE Select	NP_001361757.1:p.Pro1342Leu
NM_017519.3:c.3866C>T	NP_059989.3:p.Pro1289Leu