Canonical Allele Identifier: CA366235266

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511236A>T (hg19) ; chr6:g.157190102A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190102A>T , CM000668.2:g.157190102A>T	GRCh38
NC_000006.11:g.157511236A>T , CM000668.1:g.157511236A>T	GRCh37
NC_000006.10:g.157552928A>T	NCBI36
NG_032093.1:g.417173A>T
NG_032093.2:g.417173A>T
NG_066624.1:g.419077A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3964A>T	ENSP00000055163.8:p.Asn1322Tyr
ENST00000414678.8:c.4033A>T	ENSP00000412835.3:p.Asn1345Tyr
ENST00000637015.2:c.4252A>T	ENSP00000489729.2:p.Asn1418Tyr
ENST00000346085.10:c.4003A>T	ENSP00000344546.5:p.Asn1335Tyr
ENST00000350026.10:c.3715A>T	ENSP00000055163.7:p.Asn1239Tyr
ENST00000414678.7:c.2281A>T	ENSP00000412835.2:p.Asn761Tyr
ENST00000635849.1:c.1444A>T	ENSP00000490948.1:p.Asn482Tyr
ENST00000635957.1:c.1075A>T	ENSP00000490385.1:p.Asn359Tyr
ENST00000636930.2:c.4123A>T MANE Select	ENSP00000490491.2:p.Asn1375Tyr
ENST00000636940.1:n.2120A>T
ENST00000637015.1:c.1491A>T
ENST00000637568.1:c.1405A>T
ENST00000637741.1:n.789A>T
ENST00000637810.1:c.1465A>T	ENSP00000489636.1:p.Asn489Tyr
ENST00000637904.1:c.1624A>T	ENSP00000490550.1:p.Asn542Tyr
ENST00000647938.1:c.3754A>T	ENSP00000498155.1:p.Asn1252Tyr
ENST00000346085.9:c.3754A>T	ENSP00000344546.4:p.Asn1252Tyr
ENST00000350026.9:c.3715A>T	ENSP00000055163.7:p.Asn1239Tyr
ENST00000414678.6:c.2281A>T	ENSP00000412835.2:p.Asn761Tyr
NM_017519.2:c.3715A>T	NP_059989.2:p.Asn1239Tyr
NM_020732.3:c.3754A>T	NP_065783.3:p.Asn1252Tyr
XM_005267069.3:c.3874A>T	XP_005267126.2:p.Asn1292Tyr
XM_011535984.1:c.2953A>T	XP_011534286.1:p.Asn985Tyr
XM_011535985.1:c.2773A>T	XP_011534287.1:p.Asn925Tyr
XM_011535986.1:c.2533A>T	XP_011534288.1:p.Asn845Tyr
XM_011535987.1:c.2152A>T	XP_011534289.1:p.Asn718Tyr
XM_011535988.1:c.1015A>T	XP_011534290.1:p.Asn339Tyr
NM_001346813.1:c.3874A>T	NP_001333742.1:p.Asn1292Tyr
NM_001363725.1:c.1624A>T	NP_001350654.1:p.Asn542Tyr
XM_011535984.2:c.4084A>T	XP_011534286.2:p.Asn1362Tyr
XM_011535988.3:c.1015A>T	XP_011534290.1:p.Asn339Tyr
XM_017011103.2:c.3985A>T	XP_016866592.1:p.Asn1329Tyr
XM_017011104.1:c.3955A>T	XP_016866593.1:p.Asn1319Tyr
XM_017011105.2:c.3925A>T	XP_016866594.1:p.Asn1309Tyr
XM_017011106.2:c.3796A>T	XP_016866595.1:p.Asn1266Tyr
XM_017011107.2:c.3775A>T	XP_016866596.1:p.Asn1259Tyr
XR_002956289.1:n.4167A>T
NM_001363725.2:c.1624A>T	NP_001350654.1:p.Asn542Tyr
NM_001371656.1:c.4003A>T	NP_001358585.1:p.Asn1335Tyr
NM_001374820.1:c.4003A>T	NP_001361749.1:p.Asn1335Tyr
NM_001374828.1:c.4123A>T MANE Select	NP_001361757.1:p.Asn1375Tyr
NM_017519.3:c.3964A>T	NP_059989.3:p.Asn1322Tyr