Canonical Allele Identifier: CA4067521

Gene: ARID1B

Linked Data

• dbSNP Id: rs773649998
• ExAC: 6:157511209 G / A
• gnomAD v2: 6-157511209-G-A
• gnomAD v4: 6-157190075-G-A
• MyVariant Identifiers: chr6:g.157511209G>A (hg19) ; chr6:g.157190075G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190075G>A , CM000668.2:g.157190075G>A	GRCh38
NC_000006.11:g.157511209G>A , CM000668.1:g.157511209G>A	GRCh37
NC_000006.10:g.157552901G>A	NCBI36
NG_032093.1:g.417146G>A
NG_032093.2:g.417146G>A
NG_066624.1:g.419050G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3937G>A	ENSP00000055163.8:p.Val1313Met
ENST00000414678.8:c.4006G>A	ENSP00000412835.3:p.Val1336Met
ENST00000637015.2:c.4225G>A	ENSP00000489729.2:p.Val1409Met
ENST00000346085.10:c.3976G>A	ENSP00000344546.5:p.Val1326Met
ENST00000350026.10:c.3688G>A	ENSP00000055163.7:p.Val1230Met
ENST00000414678.7:c.2254G>A	ENSP00000412835.2:p.Val752Met
ENST00000635849.1:c.1417G>A	ENSP00000490948.1:p.Val473Met
ENST00000635957.1:c.1048G>A	ENSP00000490385.1:p.Val350Met
ENST00000636930.2:c.4096G>A MANE Select	ENSP00000490491.2:p.Val1366Met
ENST00000636940.1:n.2093G>A
ENST00000637015.1:c.1464G>A
ENST00000637568.1:c.1378G>A
ENST00000637741.1:n.762G>A
ENST00000637810.1:c.1438G>A	ENSP00000489636.1:p.Val480Met
ENST00000637904.1:c.1597G>A	ENSP00000490550.1:p.Val533Met
ENST00000647938.1:c.3727G>A	ENSP00000498155.1:p.Val1243Met
ENST00000346085.9:c.3727G>A	ENSP00000344546.4:p.Val1243Met
ENST00000350026.9:c.3688G>A	ENSP00000055163.7:p.Val1230Met
ENST00000414678.6:c.2254G>A	ENSP00000412835.2:p.Val752Met
NM_017519.2:c.3688G>A	NP_059989.2:p.Val1230Met
NM_020732.3:c.3727G>A	NP_065783.3:p.Val1243Met
XM_005267069.3:c.3847G>A	XP_005267126.2:p.Val1283Met
XM_011535984.1:c.2926G>A	XP_011534286.1:p.Val976Met
XM_011535985.1:c.2746G>A	XP_011534287.1:p.Val916Met
XM_011535986.1:c.2506G>A	XP_011534288.1:p.Val836Met
XM_011535987.1:c.2125G>A	XP_011534289.1:p.Val709Met
XM_011535988.1:c.988G>A	XP_011534290.1:p.Val330Met
NM_001346813.1:c.3847G>A	NP_001333742.1:p.Val1283Met
NM_001363725.1:c.1597G>A	NP_001350654.1:p.Val533Met
XM_011535984.2:c.4057G>A	XP_011534286.2:p.Val1353Met
XM_011535988.3:c.988G>A	XP_011534290.1:p.Val330Met
XM_017011103.2:c.3958G>A	XP_016866592.1:p.Val1320Met
XM_017011104.1:c.3928G>A	XP_016866593.1:p.Val1310Met
XM_017011105.2:c.3898G>A	XP_016866594.1:p.Val1300Met
XM_017011106.2:c.3769G>A	XP_016866595.1:p.Val1257Met
XM_017011107.2:c.3748G>A	XP_016866596.1:p.Val1250Met
XR_002956289.1:n.4140G>A
NM_001363725.2:c.1597G>A	NP_001350654.1:p.Val533Met
NM_001371656.1:c.3976G>A	NP_001358585.1:p.Val1326Met
NM_001374820.1:c.3976G>A	NP_001361749.1:p.Val1326Met
NM_001374828.1:c.4096G>A MANE Select	NP_001361757.1:p.Val1366Met
NM_017519.3:c.3937G>A	NP_059989.3:p.Val1313Met