Canonical Allele Identifier: CA366241417

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522134A>T (hg19) ; chr6:g.157201000A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201000A>T , CM000668.2:g.157201000A>T	GRCh38
NC_000006.11:g.157522134A>T , CM000668.1:g.157522134A>T	GRCh37
NC_000006.10:g.157563826A>T	NCBI36
NG_032093.1:g.428071A>T
NG_032093.2:g.428071A>T
NG_066624.1:g.429975A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4616A>T	ENSP00000055163.8:p.Asn1539Ile
ENST00000414678.8:c.4685A>T	ENSP00000412835.3:p.Asn1562Ile
ENST00000637015.2:c.4904A>T	ENSP00000489729.2:p.Asn1635Ile
ENST00000346085.10:c.4655A>T	ENSP00000344546.5:p.Asn1552Ile
ENST00000350026.10:c.4367A>T	ENSP00000055163.7:p.Asn1456Ile
ENST00000414678.7:c.2933A>T	ENSP00000412835.2:p.Asn978Ile
ENST00000635849.1:c.2096A>T	ENSP00000490948.1:p.Asn699Ile
ENST00000635957.1:c.1727A>T	ENSP00000490385.1:p.Asn576Ile
ENST00000636227.1:n.3238A>T
ENST00000636254.1:n.695A>T
ENST00000636930.2:c.4775A>T MANE Select	ENSP00000490491.2:p.Asn1592Ile
ENST00000636940.1:n.2772A>T
ENST00000637015.1:c.2143A>T
ENST00000637568.1:c.2057A>T
ENST00000637741.1:n.1441A>T
ENST00000637810.1:c.2117A>T	ENSP00000489636.1:p.Asn706Ile
ENST00000637904.1:c.2276A>T	ENSP00000490550.1:p.Asn759Ile
ENST00000647938.1:c.4406A>T	ENSP00000498155.1:p.Asn1469Ile
ENST00000346085.9:c.4406A>T	ENSP00000344546.4:p.Asn1469Ile
ENST00000350026.9:c.4367A>T	ENSP00000055163.7:p.Asn1456Ile
ENST00000414678.6:c.2933A>T	ENSP00000412835.2:p.Asn978Ile
NM_017519.2:c.4367A>T	NP_059989.2:p.Asn1456Ile
NM_020732.3:c.4406A>T	NP_065783.3:p.Asn1469Ile
XM_005267069.3:c.4526A>T	XP_005267126.2:p.Asn1509Ile
XM_011535984.1:c.3605A>T	XP_011534286.1:p.Asn1202Ile
XM_011535985.1:c.3425A>T	XP_011534287.1:p.Asn1142Ile
XM_011535986.1:c.3185A>T	XP_011534288.1:p.Asn1062Ile
XM_011535987.1:c.2804A>T	XP_011534289.1:p.Asn935Ile
XM_011535988.1:c.1667A>T	XP_011534290.1:p.Asn556Ile
NM_001346813.1:c.4526A>T	NP_001333742.1:p.Asn1509Ile
NM_001363725.1:c.2276A>T	NP_001350654.1:p.Asn759Ile
XM_011535984.2:c.4736A>T	XP_011534286.2:p.Asn1579Ile
XM_011535988.3:c.1667A>T	XP_011534290.1:p.Asn556Ile
XM_017011103.2:c.4637A>T	XP_016866592.1:p.Asn1546Ile
XM_017011104.1:c.4607A>T	XP_016866593.1:p.Asn1536Ile
XM_017011105.2:c.4577A>T	XP_016866594.1:p.Asn1526Ile
XM_017011106.2:c.4448A>T	XP_016866595.1:p.Asn1483Ile
XM_017011107.2:c.4427A>T	XP_016866596.1:p.Asn1476Ile
XR_002956289.1:n.4722A>T
NM_001363725.2:c.2276A>T	NP_001350654.1:p.Asn759Ile
NM_001371656.1:c.4655A>T	NP_001358585.1:p.Asn1552Ile
NM_001374820.1:c.4655A>T	NP_001361749.1:p.Asn1552Ile
NM_001374828.1:c.4775A>T MANE Select	NP_001361757.1:p.Asn1592Ile
NM_017519.3:c.4616A>T	NP_059989.3:p.Asn1539Ile