Canonical Allele Identifier: CA366242413

Gene: ARID1B

Linked Data

• dbSNP Id: rs367764610
• MyVariant Identifiers: chr6:g.157522422A>T (hg19) ; chr6:g.157201288A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201288A>T , CM000668.2:g.157201288A>T	GRCh38
NC_000006.11:g.157522422A>T , CM000668.1:g.157522422A>T	GRCh37
NC_000006.10:g.157564114A>T	NCBI36
NG_032093.1:g.428359A>T
NG_032093.2:g.428359A>T
NG_066624.1:g.430263A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4904A>T	ENSP00000055163.8:p.Asn1635Ile
ENST00000414678.8:c.4973A>T	ENSP00000412835.3:p.Asn1658Ile
ENST00000637015.2:c.5192A>T	ENSP00000489729.2:p.Asn1731Ile
ENST00000346085.10:c.4943A>T	ENSP00000344546.5:p.Asn1648Ile
ENST00000350026.10:c.4655A>T	ENSP00000055163.7:p.Asn1552Ile
ENST00000414678.7:c.3221A>T	ENSP00000412835.2:p.Asn1074Ile
ENST00000635849.1:c.2384A>T	ENSP00000490948.1:p.Asn795Ile
ENST00000635957.1:c.2015A>T	ENSP00000490385.1:p.Asn672Ile
ENST00000636227.1:n.3526A>T
ENST00000636254.1:n.983A>T
ENST00000636930.2:c.5063A>T MANE Select	ENSP00000490491.2:p.Asn1688Ile
ENST00000636940.1:n.3060A>T
ENST00000637015.1:c.2431A>T
ENST00000637568.1:c.2345A>T
ENST00000637741.1:n.1729A>T
ENST00000637810.1:c.2405A>T	ENSP00000489636.1:p.Asn802Ile
ENST00000637904.1:c.2564A>T	ENSP00000490550.1:p.Asn855Ile
ENST00000647938.1:c.4694A>T	ENSP00000498155.1:p.Asn1565Ile
ENST00000346085.9:c.4694A>T	ENSP00000344546.4:p.Asn1565Ile
ENST00000350026.9:c.4655A>T	ENSP00000055163.7:p.Asn1552Ile
ENST00000414678.6:c.3221A>T	ENSP00000412835.2:p.Asn1074Ile
NM_017519.2:c.4655A>T	NP_059989.2:p.Asn1552Ile
NM_020732.3:c.4694A>T	NP_065783.3:p.Asn1565Ile
XM_005267069.3:c.4814A>T	XP_005267126.2:p.Asn1605Ile
XM_011535984.1:c.3893A>T	XP_011534286.1:p.Asn1298Ile
XM_011535985.1:c.3713A>T	XP_011534287.1:p.Asn1238Ile
XM_011535986.1:c.3473A>T	XP_011534288.1:p.Asn1158Ile
XM_011535987.1:c.3092A>T	XP_011534289.1:p.Asn1031Ile
XM_011535988.1:c.1955A>T	XP_011534290.1:p.Asn652Ile
NM_001346813.1:c.4814A>T	NP_001333742.1:p.Asn1605Ile
NM_001363725.1:c.2564A>T	NP_001350654.1:p.Asn855Ile
XM_011535984.2:c.5024A>T	XP_011534286.2:p.Asn1675Ile
XM_011535988.3:c.1955A>T	XP_011534290.1:p.Asn652Ile
XM_017011103.2:c.4925A>T	XP_016866592.1:p.Asn1642Ile
XM_017011104.1:c.4895A>T	XP_016866593.1:p.Asn1632Ile
XM_017011105.2:c.4865A>T	XP_016866594.1:p.Asn1622Ile
XM_017011106.2:c.4736A>T	XP_016866595.1:p.Asn1579Ile
XM_017011107.2:c.4715A>T	XP_016866596.1:p.Asn1572Ile
XR_002956289.1:n.5010A>T
NM_001363725.2:c.2564A>T	NP_001350654.1:p.Asn855Ile
NM_001371656.1:c.4943A>T	NP_001358585.1:p.Asn1648Ile
NM_001374820.1:c.4943A>T	NP_001361749.1:p.Asn1648Ile
NM_001374828.1:c.5063A>T MANE Select	NP_001361757.1:p.Asn1688Ile
NM_017519.3:c.4904A>T	NP_059989.3:p.Asn1635Ile