Canonical Allele Identifier: CA366235261

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3964A>C	ENSP00000055163.8:p.Asn1322His
ENST00000414678.8:c.4033A>C	ENSP00000412835.3:p.Asn1345His
ENST00000637015.2:c.4252A>C	ENSP00000489729.2:p.Asn1418His
ENST00000346085.10:c.4003A>C	ENSP00000344546.5:p.Asn1335His
ENST00000350026.10:c.3715A>C	ENSP00000055163.7:p.Asn1239His
ENST00000414678.7:c.2281A>C	ENSP00000412835.2:p.Asn761His
ENST00000635849.1:c.1444A>C	ENSP00000490948.1:p.Asn482His
ENST00000635957.1:c.1075A>C	ENSP00000490385.1:p.Asn359His
ENST00000636930.2:c.4123A>C MANE Select	ENSP00000490491.2:p.Asn1375His
ENST00000636940.1:n.2120A>C
ENST00000637015.1:c.1491A>C
ENST00000637568.1:c.1405A>C
ENST00000637741.1:n.789A>C
ENST00000637810.1:c.1465A>C	ENSP00000489636.1:p.Asn489His
ENST00000637904.1:c.1624A>C	ENSP00000490550.1:p.Asn542His
ENST00000647938.1:c.3754A>C	ENSP00000498155.1:p.Asn1252His
ENST00000346085.9:c.3754A>C	ENSP00000344546.4:p.Asn1252His
ENST00000350026.9:c.3715A>C	ENSP00000055163.7:p.Asn1239His
ENST00000414678.6:c.2281A>C	ENSP00000412835.2:p.Asn761His
NM_017519.2:c.3715A>C	NP_059989.2:p.Asn1239His
NM_020732.3:c.3754A>C	NP_065783.3:p.Asn1252His
XM_005267069.3:c.3874A>C	XP_005267126.2:p.Asn1292His
XM_011535984.1:c.2953A>C	XP_011534286.1:p.Asn985His
XM_011535985.1:c.2773A>C	XP_011534287.1:p.Asn925His
XM_011535986.1:c.2533A>C	XP_011534288.1:p.Asn845His
XM_011535987.1:c.2152A>C	XP_011534289.1:p.Asn718His
XM_011535988.1:c.1015A>C	XP_011534290.1:p.Asn339His
NM_001346813.1:c.3874A>C	NP_001333742.1:p.Asn1292His
NM_001363725.1:c.1624A>C	NP_001350654.1:p.Asn542His
XM_011535984.2:c.4084A>C	XP_011534286.2:p.Asn1362His
XM_011535988.3:c.1015A>C	XP_011534290.1:p.Asn339His
XM_017011103.2:c.3985A>C	XP_016866592.1:p.Asn1329His
XM_017011104.1:c.3955A>C	XP_016866593.1:p.Asn1319His
XM_017011105.2:c.3925A>C	XP_016866594.1:p.Asn1309His
XM_017011106.2:c.3796A>C	XP_016866595.1:p.Asn1266His
XM_017011107.2:c.3775A>C	XP_016866596.1:p.Asn1259His
XR_002956289.1:n.4167A>C
NM_001363725.2:c.1624A>C	NP_001350654.1:p.Asn542His
NM_001371656.1:c.4003A>C	NP_001358585.1:p.Asn1335His
NM_001374820.1:c.4003A>C	NP_001361749.1:p.Asn1335His
NM_001374828.1:c.4123A>C MANE Select	NP_001361757.1:p.Asn1375His
NM_017519.3:c.3964A>C	NP_059989.3:p.Asn1322His