Canonical Allele Identifier: CA366234302

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510899C>G (hg19) ; chr6:g.157189765C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189765C>G , CM000668.2:g.157189765C>G	GRCh38
NC_000006.11:g.157510899C>G , CM000668.1:g.157510899C>G	GRCh37
NC_000006.10:g.157552591C>G	NCBI36
NG_032093.1:g.416836C>G
NG_032093.2:g.416836C>G
NG_066624.1:g.418740C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3884C>G	ENSP00000055163.8:p.Pro1295Arg
ENST00000414678.8:c.3953C>G	ENSP00000412835.3:p.Pro1318Arg
ENST00000637015.2:c.4172C>G	ENSP00000489729.2:p.Pro1391Arg
ENST00000346085.10:c.3923C>G	ENSP00000344546.5:p.Pro1308Arg
ENST00000350026.10:c.3635C>G	ENSP00000055163.7:p.Pro1212Arg
ENST00000414678.7:c.2201C>G	ENSP00000412835.2:p.Pro734Arg
ENST00000635849.1:c.1364C>G	ENSP00000490948.1:p.Pro455Arg
ENST00000635957.1:c.998C>G	ENSP00000490385.1:p.Pro333Arg
ENST00000636930.2:c.4043C>G MANE Select	ENSP00000490491.2:p.Pro1348Arg
ENST00000636940.1:n.2040C>G
ENST00000637015.1:c.1411C>G
ENST00000637568.1:c.1325C>G
ENST00000637741.1:n.709C>G
ENST00000637810.1:c.1385C>G	ENSP00000489636.1:p.Pro462Arg
ENST00000637904.1:c.1544C>G	ENSP00000490550.1:p.Pro515Arg
ENST00000647938.1:c.3674C>G	ENSP00000498155.1:p.Pro1225Arg
ENST00000346085.9:c.3674C>G	ENSP00000344546.4:p.Pro1225Arg
ENST00000350026.9:c.3635C>G	ENSP00000055163.7:p.Pro1212Arg
ENST00000414678.6:c.2201C>G	ENSP00000412835.2:p.Pro734Arg
NM_017519.2:c.3635C>G	NP_059989.2:p.Pro1212Arg
NM_020732.3:c.3674C>G	NP_065783.3:p.Pro1225Arg
XM_005267069.3:c.3794C>G	XP_005267126.2:p.Pro1265Arg
XM_011535984.1:c.2873C>G	XP_011534286.1:p.Pro958Arg
XM_011535985.1:c.2693C>G	XP_011534287.1:p.Pro898Arg
XM_011535986.1:c.2453C>G	XP_011534288.1:p.Pro818Arg
XM_011535987.1:c.2072C>G	XP_011534289.1:p.Pro691Arg
XM_011535988.1:c.935C>G	XP_011534290.1:p.Pro312Arg
NM_001346813.1:c.3794C>G	NP_001333742.1:p.Pro1265Arg
NM_001363725.1:c.1544C>G	NP_001350654.1:p.Pro515Arg
XM_011535984.2:c.4004C>G	XP_011534286.2:p.Pro1335Arg
XM_011535988.3:c.935C>G	XP_011534290.1:p.Pro312Arg
XM_017011103.2:c.3905C>G	XP_016866592.1:p.Pro1302Arg
XM_017011104.1:c.3875C>G	XP_016866593.1:p.Pro1292Arg
XM_017011105.2:c.3845C>G	XP_016866594.1:p.Pro1282Arg
XM_017011106.2:c.3716C>G	XP_016866595.1:p.Pro1239Arg
XM_017011107.2:c.3695C>G	XP_016866596.1:p.Pro1232Arg
XR_002956289.1:n.4087C>G
NM_001363725.2:c.1544C>G	NP_001350654.1:p.Pro515Arg
NM_001371656.1:c.3923C>G	NP_001358585.1:p.Pro1308Arg
NM_001374820.1:c.3923C>G	NP_001361749.1:p.Pro1308Arg
NM_001374828.1:c.4043C>G MANE Select	NP_001361757.1:p.Pro1348Arg
NM_017519.3:c.3884C>G	NP_059989.3:p.Pro1295Arg