Canonical Allele Identifier: CA366234177

Gene: ARID1B

Linked Data

• dbSNP Id: rs901157371
• MyVariant Identifiers: chr6:g.157510863C>A (hg19) ; chr6:g.157189729C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189729C>A , CM000668.2:g.157189729C>A	GRCh38
NC_000006.11:g.157510863C>A , CM000668.1:g.157510863C>A	GRCh37
NC_000006.10:g.157552555C>A	NCBI36
NG_032093.1:g.416800C>A
NG_032093.2:g.416800C>A
NG_066624.1:g.418704C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3848C>A	ENSP00000055163.8:p.Pro1283His
ENST00000414678.8:c.3917C>A	ENSP00000412835.3:p.Pro1306His
ENST00000637015.2:c.4136C>A	ENSP00000489729.2:p.Pro1379His
ENST00000346085.10:c.3887C>A	ENSP00000344546.5:p.Pro1296His
ENST00000350026.10:c.3599C>A	ENSP00000055163.7:p.Pro1200His
ENST00000414678.7:c.2165C>A	ENSP00000412835.2:p.Pro722His
ENST00000635849.1:c.1328C>A	ENSP00000490948.1:p.Pro443His
ENST00000635957.1:c.962C>A	ENSP00000490385.1:p.Pro321His
ENST00000636930.2:c.4007C>A MANE Select	ENSP00000490491.2:p.Pro1336His
ENST00000636940.1:n.2004C>A
ENST00000637015.1:c.1375C>A
ENST00000637568.1:c.1289C>A
ENST00000637741.1:n.673C>A
ENST00000637810.1:c.1349C>A	ENSP00000489636.1:p.Pro450His
ENST00000637904.1:c.1508C>A	ENSP00000490550.1:p.Pro503His
ENST00000647938.1:c.3638C>A	ENSP00000498155.1:p.Pro1213His
ENST00000346085.9:c.3638C>A	ENSP00000344546.4:p.Pro1213His
ENST00000350026.9:c.3599C>A	ENSP00000055163.7:p.Pro1200His
ENST00000414678.6:c.2165C>A	ENSP00000412835.2:p.Pro722His
NM_017519.2:c.3599C>A	NP_059989.2:p.Pro1200His
NM_020732.3:c.3638C>A	NP_065783.3:p.Pro1213His
XM_005267069.3:c.3758C>A	XP_005267126.2:p.Pro1253His
XM_011535984.1:c.2837C>A	XP_011534286.1:p.Pro946His
XM_011535985.1:c.2657C>A	XP_011534287.1:p.Pro886His
XM_011535986.1:c.2417C>A	XP_011534288.1:p.Pro806His
XM_011535987.1:c.2036C>A	XP_011534289.1:p.Pro679His
XM_011535988.1:c.899C>A	XP_011534290.1:p.Pro300His
NM_001346813.1:c.3758C>A	NP_001333742.1:p.Pro1253His
NM_001363725.1:c.1508C>A	NP_001350654.1:p.Pro503His
XM_011535984.2:c.3968C>A	XP_011534286.2:p.Pro1323His
XM_011535988.3:c.899C>A	XP_011534290.1:p.Pro300His
XM_017011103.2:c.3869C>A	XP_016866592.1:p.Pro1290His
XM_017011104.1:c.3839C>A	XP_016866593.1:p.Pro1280His
XM_017011105.2:c.3809C>A	XP_016866594.1:p.Pro1270His
XM_017011106.2:c.3680C>A	XP_016866595.1:p.Pro1227His
XM_017011107.2:c.3659C>A	XP_016866596.1:p.Pro1220His
XR_002956289.1:n.4051C>A
NM_001363725.2:c.1508C>A	NP_001350654.1:p.Pro503His
NM_001371656.1:c.3887C>A	NP_001358585.1:p.Pro1296His
NM_001374820.1:c.3887C>A	NP_001361749.1:p.Pro1296His
NM_001374828.1:c.4007C>A MANE Select	NP_001361757.1:p.Pro1336His
NM_017519.3:c.3848C>A	NP_059989.3:p.Pro1283His