Canonical Allele Identifier: CA366234088

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510821G>T (hg19) ; chr6:g.157189687G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189687G>T , CM000668.2:g.157189687G>T	GRCh38
NC_000006.11:g.157510821G>T , CM000668.1:g.157510821G>T	GRCh37
NC_000006.10:g.157552513G>T	NCBI36
NG_032093.1:g.416758G>T
NG_032093.2:g.416758G>T
NG_066624.1:g.418662G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3806G>T	ENSP00000055163.8:p.Gly1269Val
ENST00000414678.8:c.3875G>T	ENSP00000412835.3:p.Gly1292Val
ENST00000637015.2:c.4094G>T	ENSP00000489729.2:p.Gly1365Val
ENST00000346085.10:c.3845G>T	ENSP00000344546.5:p.Gly1282Val
ENST00000350026.10:c.3557G>T	ENSP00000055163.7:p.Gly1186Val
ENST00000414678.7:c.2123G>T	ENSP00000412835.2:p.Gly708Val
ENST00000635849.1:c.1286G>T	ENSP00000490948.1:p.Gly429Val
ENST00000635957.1:c.920G>T	ENSP00000490385.1:p.Gly307Val
ENST00000636930.2:c.3965G>T MANE Select	ENSP00000490491.2:p.Gly1322Val
ENST00000636940.1:n.1962G>T
ENST00000637015.1:c.1333G>T
ENST00000637568.1:c.1247G>T
ENST00000637741.1:n.631G>T
ENST00000637810.1:c.1307G>T	ENSP00000489636.1:p.Gly436Val
ENST00000637904.1:c.1466G>T	ENSP00000490550.1:p.Gly489Val
ENST00000647938.1:c.3596G>T	ENSP00000498155.1:p.Gly1199Val
ENST00000346085.9:c.3596G>T	ENSP00000344546.4:p.Gly1199Val
ENST00000350026.9:c.3557G>T	ENSP00000055163.7:p.Gly1186Val
ENST00000414678.6:c.2123G>T	ENSP00000412835.2:p.Gly708Val
NM_017519.2:c.3557G>T	NP_059989.2:p.Gly1186Val
NM_020732.3:c.3596G>T	NP_065783.3:p.Gly1199Val
XM_005267069.3:c.3716G>T	XP_005267126.2:p.Gly1239Val
XM_011535984.1:c.2795G>T	XP_011534286.1:p.Gly932Val
XM_011535985.1:c.2615G>T	XP_011534287.1:p.Gly872Val
XM_011535986.1:c.2375G>T	XP_011534288.1:p.Gly792Val
XM_011535987.1:c.1994G>T	XP_011534289.1:p.Gly665Val
XM_011535988.1:c.857G>T	XP_011534290.1:p.Gly286Val
NM_001346813.1:c.3716G>T	NP_001333742.1:p.Gly1239Val
NM_001363725.1:c.1466G>T	NP_001350654.1:p.Gly489Val
XM_011535984.2:c.3926G>T	XP_011534286.2:p.Gly1309Val
XM_011535988.3:c.857G>T	XP_011534290.1:p.Gly286Val
XM_017011103.2:c.3827G>T	XP_016866592.1:p.Gly1276Val
XM_017011104.1:c.3797G>T	XP_016866593.1:p.Gly1266Val
XM_017011105.2:c.3767G>T	XP_016866594.1:p.Gly1256Val
XM_017011106.2:c.3638G>T	XP_016866595.1:p.Gly1213Val
XM_017011107.2:c.3617G>T	XP_016866596.1:p.Gly1206Val
XR_002956289.1:n.4009G>T
NM_001363725.2:c.1466G>T	NP_001350654.1:p.Gly489Val
NM_001371656.1:c.3845G>T	NP_001358585.1:p.Gly1282Val
NM_001374820.1:c.3845G>T	NP_001361749.1:p.Gly1282Val
NM_001374828.1:c.3965G>T MANE Select	NP_001361757.1:p.Gly1322Val
NM_017519.3:c.3806G>T	NP_059989.3:p.Gly1269Val