Canonical Allele Identifier: CA366235263

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3964A>G	ENSP00000055163.8:p.Asn1322Asp
ENST00000414678.8:c.4033A>G	ENSP00000412835.3:p.Asn1345Asp
ENST00000637015.2:c.4252A>G	ENSP00000489729.2:p.Asn1418Asp
ENST00000346085.10:c.4003A>G	ENSP00000344546.5:p.Asn1335Asp
ENST00000350026.10:c.3715A>G	ENSP00000055163.7:p.Asn1239Asp
ENST00000414678.7:c.2281A>G	ENSP00000412835.2:p.Asn761Asp
ENST00000635849.1:c.1444A>G	ENSP00000490948.1:p.Asn482Asp
ENST00000635957.1:c.1075A>G	ENSP00000490385.1:p.Asn359Asp
ENST00000636930.2:c.4123A>G MANE Select	ENSP00000490491.2:p.Asn1375Asp
ENST00000636940.1:n.2120A>G
ENST00000637015.1:c.1491A>G
ENST00000637568.1:c.1405A>G
ENST00000637741.1:n.789A>G
ENST00000637810.1:c.1465A>G	ENSP00000489636.1:p.Asn489Asp
ENST00000637904.1:c.1624A>G	ENSP00000490550.1:p.Asn542Asp
ENST00000647938.1:c.3754A>G	ENSP00000498155.1:p.Asn1252Asp
ENST00000346085.9:c.3754A>G	ENSP00000344546.4:p.Asn1252Asp
ENST00000350026.9:c.3715A>G	ENSP00000055163.7:p.Asn1239Asp
ENST00000414678.6:c.2281A>G	ENSP00000412835.2:p.Asn761Asp
NM_017519.2:c.3715A>G	NP_059989.2:p.Asn1239Asp
NM_020732.3:c.3754A>G	NP_065783.3:p.Asn1252Asp
XM_005267069.3:c.3874A>G	XP_005267126.2:p.Asn1292Asp
XM_011535984.1:c.2953A>G	XP_011534286.1:p.Asn985Asp
XM_011535985.1:c.2773A>G	XP_011534287.1:p.Asn925Asp
XM_011535986.1:c.2533A>G	XP_011534288.1:p.Asn845Asp
XM_011535987.1:c.2152A>G	XP_011534289.1:p.Asn718Asp
XM_011535988.1:c.1015A>G	XP_011534290.1:p.Asn339Asp
NM_001346813.1:c.3874A>G	NP_001333742.1:p.Asn1292Asp
NM_001363725.1:c.1624A>G	NP_001350654.1:p.Asn542Asp
XM_011535984.2:c.4084A>G	XP_011534286.2:p.Asn1362Asp
XM_011535988.3:c.1015A>G	XP_011534290.1:p.Asn339Asp
XM_017011103.2:c.3985A>G	XP_016866592.1:p.Asn1329Asp
XM_017011104.1:c.3955A>G	XP_016866593.1:p.Asn1319Asp
XM_017011105.2:c.3925A>G	XP_016866594.1:p.Asn1309Asp
XM_017011106.2:c.3796A>G	XP_016866595.1:p.Asn1266Asp
XM_017011107.2:c.3775A>G	XP_016866596.1:p.Asn1259Asp
XR_002956289.1:n.4167A>G
NM_001363725.2:c.1624A>G	NP_001350654.1:p.Asn542Asp
NM_001371656.1:c.4003A>G	NP_001358585.1:p.Asn1335Asp
NM_001374820.1:c.4003A>G	NP_001361749.1:p.Asn1335Asp
NM_001374828.1:c.4123A>G MANE Select	NP_001361757.1:p.Asn1375Asp
NM_017519.3:c.3964A>G	NP_059989.3:p.Asn1322Asp