Canonical Allele Identifier: CA366234317

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3884C>A	ENSP00000055163.8:p.Pro1295Gln
ENST00000414678.8:c.3953C>A	ENSP00000412835.3:p.Pro1318Gln
ENST00000637015.2:c.4172C>A	ENSP00000489729.2:p.Pro1391Gln
ENST00000346085.10:c.3923C>A	ENSP00000344546.5:p.Pro1308Gln
ENST00000350026.10:c.3635C>A	ENSP00000055163.7:p.Pro1212Gln
ENST00000414678.7:c.2201C>A	ENSP00000412835.2:p.Pro734Gln
ENST00000635849.1:c.1364C>A	ENSP00000490948.1:p.Pro455Gln
ENST00000635957.1:c.998C>A	ENSP00000490385.1:p.Pro333Gln
ENST00000636930.2:c.4043C>A MANE Select	ENSP00000490491.2:p.Pro1348Gln
ENST00000636940.1:n.2040C>A
ENST00000637015.1:c.1411C>A
ENST00000637568.1:c.1325C>A
ENST00000637741.1:n.709C>A
ENST00000637810.1:c.1385C>A	ENSP00000489636.1:p.Pro462Gln
ENST00000637904.1:c.1544C>A	ENSP00000490550.1:p.Pro515Gln
ENST00000647938.1:c.3674C>A	ENSP00000498155.1:p.Pro1225Gln
ENST00000346085.9:c.3674C>A	ENSP00000344546.4:p.Pro1225Gln
ENST00000350026.9:c.3635C>A	ENSP00000055163.7:p.Pro1212Gln
ENST00000414678.6:c.2201C>A	ENSP00000412835.2:p.Pro734Gln
NM_017519.2:c.3635C>A	NP_059989.2:p.Pro1212Gln
NM_020732.3:c.3674C>A	NP_065783.3:p.Pro1225Gln
XM_005267069.3:c.3794C>A	XP_005267126.2:p.Pro1265Gln
XM_011535984.1:c.2873C>A	XP_011534286.1:p.Pro958Gln
XM_011535985.1:c.2693C>A	XP_011534287.1:p.Pro898Gln
XM_011535986.1:c.2453C>A	XP_011534288.1:p.Pro818Gln
XM_011535987.1:c.2072C>A	XP_011534289.1:p.Pro691Gln
XM_011535988.1:c.935C>A	XP_011534290.1:p.Pro312Gln
NM_001346813.1:c.3794C>A	NP_001333742.1:p.Pro1265Gln
NM_001363725.1:c.1544C>A	NP_001350654.1:p.Pro515Gln
XM_011535984.2:c.4004C>A	XP_011534286.2:p.Pro1335Gln
XM_011535988.3:c.935C>A	XP_011534290.1:p.Pro312Gln
XM_017011103.2:c.3905C>A	XP_016866592.1:p.Pro1302Gln
XM_017011104.1:c.3875C>A	XP_016866593.1:p.Pro1292Gln
XM_017011105.2:c.3845C>A	XP_016866594.1:p.Pro1282Gln
XM_017011106.2:c.3716C>A	XP_016866595.1:p.Pro1239Gln
XM_017011107.2:c.3695C>A	XP_016866596.1:p.Pro1232Gln
XR_002956289.1:n.4087C>A
NM_001363725.2:c.1544C>A	NP_001350654.1:p.Pro515Gln
NM_001371656.1:c.3923C>A	NP_001358585.1:p.Pro1308Gln
NM_001374820.1:c.3923C>A	NP_001361749.1:p.Pro1308Gln
NM_001374828.1:c.4043C>A MANE Select	NP_001361757.1:p.Pro1348Gln
NM_017519.3:c.3884C>A	NP_059989.3:p.Pro1295Gln