Canonical Allele Identifier: CA452978046

Gene: ARID1B

Linked Data

• dbSNP Id: rs1311738943
• MyVariant Identifiers: chr6:g.157522084G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200950G>T , CM000668.2:g.157200950G>T	GRCh38
NC_000006.11:g.157522084G>T , CM000668.1:g.157522084G>T	GRCh37
NC_000006.10:g.157563776G>T	NCBI36
NG_032093.1:g.428021G>T
NG_032093.2:g.428021G>T
NG_066624.1:g.429925G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4566G>T	ENSP00000055163.8:p.Leu1522=
ENST00000414678.8:c.4635G>T	ENSP00000412835.3:p.Leu1545=
ENST00000637015.2:c.4854G>T	ENSP00000489729.2:p.Leu1618=
ENST00000346085.10:c.4605G>T	ENSP00000344546.5:p.Leu1535=
ENST00000350026.10:c.4317G>T	ENSP00000055163.7:p.Leu1439=
ENST00000414678.7:c.2883G>T	ENSP00000412835.2:p.Leu961=
ENST00000635849.1:c.2046G>T	ENSP00000490948.1:p.Leu682=
ENST00000635957.1:c.1677G>T	ENSP00000490385.1:p.Leu559=
ENST00000636227.1:n.3188G>T
ENST00000636254.1:n.645G>T
ENST00000636930.2:c.4725G>T MANE Select	ENSP00000490491.2:p.Leu1575=
ENST00000636940.1:n.2722G>T
ENST00000637015.1:c.2093G>T
ENST00000637568.1:c.2007G>T
ENST00000637741.1:n.1391G>T
ENST00000637810.1:c.2067G>T	ENSP00000489636.1:p.Leu689=
ENST00000637904.1:c.2226G>T	ENSP00000490550.1:p.Leu742=
ENST00000647938.1:c.4356G>T	ENSP00000498155.1:p.Leu1452=
ENST00000346085.9:c.4356G>T	ENSP00000344546.4:p.Leu1452=
ENST00000350026.9:c.4317G>T	ENSP00000055163.7:p.Leu1439=
ENST00000414678.6:c.2883G>T	ENSP00000412835.2:p.Leu961=
NM_017519.2:c.4317G>T	NP_059989.2:p.Leu1439=
NM_020732.3:c.4356G>T	NP_065783.3:p.Leu1452=
XM_005267069.3:c.4476G>T	XP_005267126.2:p.Leu1492=
XM_011535984.1:c.3555G>T	XP_011534286.1:p.Leu1185=
XM_011535985.1:c.3375G>T	XP_011534287.1:p.Leu1125=
XM_011535986.1:c.3135G>T	XP_011534288.1:p.Leu1045=
XM_011535987.1:c.2754G>T	XP_011534289.1:p.Leu918=
XM_011535988.1:c.1617G>T	XP_011534290.1:p.Leu539=
NM_001346813.1:c.4476G>T	NP_001333742.1:p.Leu1492=
NM_001363725.1:c.2226G>T	NP_001350654.1:p.Leu742=
XM_011535984.2:c.4686G>T	XP_011534286.2:p.Leu1562=
XM_011535988.3:c.1617G>T	XP_011534290.1:p.Leu539=
XM_017011103.2:c.4587G>T	XP_016866592.1:p.Leu1529=
XM_017011104.1:c.4557G>T	XP_016866593.1:p.Leu1519=
XM_017011105.2:c.4527G>T	XP_016866594.1:p.Leu1509=
XM_017011106.2:c.4398G>T	XP_016866595.1:p.Leu1466=
XM_017011107.2:c.4377G>T	XP_016866596.1:p.Leu1459=
XR_002956289.1:n.4672G>T
NM_001363725.2:c.2226G>T	NP_001350654.1:p.Leu742=
NM_001371656.1:c.4605G>T	NP_001358585.1:p.Leu1535=
NM_001374820.1:c.4605G>T	NP_001361749.1:p.Leu1535=
NM_001374828.1:c.4725G>T MANE Select	NP_001361757.1:p.Leu1575=
NM_017519.3:c.4566G>T	NP_059989.3:p.Leu1522=