Canonical Allele Identifier: CA366241568

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522158A>T (hg19) ; chr6:g.157201024A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201024A>T , CM000668.2:g.157201024A>T	GRCh38
NC_000006.11:g.157522158A>T , CM000668.1:g.157522158A>T	GRCh37
NC_000006.10:g.157563850A>T	NCBI36
NG_032093.1:g.428095A>T
NG_032093.2:g.428095A>T
NG_066624.1:g.429999A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4640A>T	ENSP00000055163.8:p.Asn1547Ile
ENST00000414678.8:c.4709A>T	ENSP00000412835.3:p.Asn1570Ile
ENST00000637015.2:c.4928A>T	ENSP00000489729.2:p.Asn1643Ile
ENST00000346085.10:c.4679A>T	ENSP00000344546.5:p.Asn1560Ile
ENST00000350026.10:c.4391A>T	ENSP00000055163.7:p.Asn1464Ile
ENST00000414678.7:c.2957A>T	ENSP00000412835.2:p.Asn986Ile
ENST00000635849.1:c.2120A>T	ENSP00000490948.1:p.Asn707Ile
ENST00000635957.1:c.1751A>T	ENSP00000490385.1:p.Asn584Ile
ENST00000636227.1:n.3262A>T
ENST00000636254.1:n.719A>T
ENST00000636930.2:c.4799A>T MANE Select	ENSP00000490491.2:p.Asn1600Ile
ENST00000636940.1:n.2796A>T
ENST00000637015.1:c.2167A>T
ENST00000637568.1:c.2081A>T
ENST00000637741.1:n.1465A>T
ENST00000637810.1:c.2141A>T	ENSP00000489636.1:p.Asn714Ile
ENST00000637904.1:c.2300A>T	ENSP00000490550.1:p.Asn767Ile
ENST00000647938.1:c.4430A>T	ENSP00000498155.1:p.Asn1477Ile
ENST00000346085.9:c.4430A>T	ENSP00000344546.4:p.Asn1477Ile
ENST00000350026.9:c.4391A>T	ENSP00000055163.7:p.Asn1464Ile
ENST00000414678.6:c.2957A>T	ENSP00000412835.2:p.Asn986Ile
NM_017519.2:c.4391A>T	NP_059989.2:p.Asn1464Ile
NM_020732.3:c.4430A>T	NP_065783.3:p.Asn1477Ile
XM_005267069.3:c.4550A>T	XP_005267126.2:p.Asn1517Ile
XM_011535984.1:c.3629A>T	XP_011534286.1:p.Asn1210Ile
XM_011535985.1:c.3449A>T	XP_011534287.1:p.Asn1150Ile
XM_011535986.1:c.3209A>T	XP_011534288.1:p.Asn1070Ile
XM_011535987.1:c.2828A>T	XP_011534289.1:p.Asn943Ile
XM_011535988.1:c.1691A>T	XP_011534290.1:p.Asn564Ile
NM_001346813.1:c.4550A>T	NP_001333742.1:p.Asn1517Ile
NM_001363725.1:c.2300A>T	NP_001350654.1:p.Asn767Ile
XM_011535984.2:c.4760A>T	XP_011534286.2:p.Asn1587Ile
XM_011535988.3:c.1691A>T	XP_011534290.1:p.Asn564Ile
XM_017011103.2:c.4661A>T	XP_016866592.1:p.Asn1554Ile
XM_017011104.1:c.4631A>T	XP_016866593.1:p.Asn1544Ile
XM_017011105.2:c.4601A>T	XP_016866594.1:p.Asn1534Ile
XM_017011106.2:c.4472A>T	XP_016866595.1:p.Asn1491Ile
XM_017011107.2:c.4451A>T	XP_016866596.1:p.Asn1484Ile
XR_002956289.1:n.4746A>T
NM_001363725.2:c.2300A>T	NP_001350654.1:p.Asn767Ile
NM_001371656.1:c.4679A>T	NP_001358585.1:p.Asn1560Ile
NM_001374820.1:c.4679A>T	NP_001361749.1:p.Asn1560Ile
NM_001374828.1:c.4799A>T MANE Select	NP_001361757.1:p.Asn1600Ile
NM_017519.3:c.4640A>T	NP_059989.3:p.Asn1547Ile