Canonical Allele Identifier: CA366234311

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339047
• MyVariant Identifiers: chr6:g.157510899C>T (hg19) ; chr6:g.157189765C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3884C>T	ENSP00000055163.8:p.Pro1295Leu
ENST00000414678.8:c.3953C>T	ENSP00000412835.3:p.Pro1318Leu
ENST00000637015.2:c.4172C>T	ENSP00000489729.2:p.Pro1391Leu
ENST00000346085.10:c.3923C>T	ENSP00000344546.5:p.Pro1308Leu
ENST00000350026.10:c.3635C>T	ENSP00000055163.7:p.Pro1212Leu
ENST00000414678.7:c.2201C>T	ENSP00000412835.2:p.Pro734Leu
ENST00000635849.1:c.1364C>T	ENSP00000490948.1:p.Pro455Leu
ENST00000635957.1:c.998C>T	ENSP00000490385.1:p.Pro333Leu
ENST00000636930.2:c.4043C>T MANE Select	ENSP00000490491.2:p.Pro1348Leu
ENST00000636940.1:n.2040C>T
ENST00000637015.1:c.1411C>T
ENST00000637568.1:c.1325C>T
ENST00000637741.1:n.709C>T
ENST00000637810.1:c.1385C>T	ENSP00000489636.1:p.Pro462Leu
ENST00000637904.1:c.1544C>T	ENSP00000490550.1:p.Pro515Leu
ENST00000647938.1:c.3674C>T	ENSP00000498155.1:p.Pro1225Leu
ENST00000346085.9:c.3674C>T	ENSP00000344546.4:p.Pro1225Leu
ENST00000350026.9:c.3635C>T	ENSP00000055163.7:p.Pro1212Leu
ENST00000414678.6:c.2201C>T	ENSP00000412835.2:p.Pro734Leu
NM_017519.2:c.3635C>T	NP_059989.2:p.Pro1212Leu
NM_020732.3:c.3674C>T	NP_065783.3:p.Pro1225Leu
XM_005267069.3:c.3794C>T	XP_005267126.2:p.Pro1265Leu
XM_011535984.1:c.2873C>T	XP_011534286.1:p.Pro958Leu
XM_011535985.1:c.2693C>T	XP_011534287.1:p.Pro898Leu
XM_011535986.1:c.2453C>T	XP_011534288.1:p.Pro818Leu
XM_011535987.1:c.2072C>T	XP_011534289.1:p.Pro691Leu
XM_011535988.1:c.935C>T	XP_011534290.1:p.Pro312Leu
NM_001346813.1:c.3794C>T	NP_001333742.1:p.Pro1265Leu
NM_001363725.1:c.1544C>T	NP_001350654.1:p.Pro515Leu
XM_011535984.2:c.4004C>T	XP_011534286.2:p.Pro1335Leu
XM_011535988.3:c.935C>T	XP_011534290.1:p.Pro312Leu
XM_017011103.2:c.3905C>T	XP_016866592.1:p.Pro1302Leu
XM_017011104.1:c.3875C>T	XP_016866593.1:p.Pro1292Leu
XM_017011105.2:c.3845C>T	XP_016866594.1:p.Pro1282Leu
XM_017011106.2:c.3716C>T	XP_016866595.1:p.Pro1239Leu
XM_017011107.2:c.3695C>T	XP_016866596.1:p.Pro1232Leu
XR_002956289.1:n.4087C>T
NM_001363725.2:c.1544C>T	NP_001350654.1:p.Pro515Leu
NM_001371656.1:c.3923C>T	NP_001358585.1:p.Pro1308Leu
NM_001374820.1:c.3923C>T	NP_001361749.1:p.Pro1308Leu
NM_001374828.1:c.4043C>T MANE Select	NP_001361757.1:p.Pro1348Leu
NM_017519.3:c.3884C>T	NP_059989.3:p.Pro1295Leu