Canonical Allele Identifier: CA4067709

Gene: ARID1B

Linked Data

• dbSNP Id: rs748759595
• ExAC: 6:157522137 A / T
• gnomAD v2: 6-157522137-A-T
• gnomAD v4: 6-157201003-A-T
• MyVariant Identifiers: chr6:g.157522137A>T (hg19) ; chr6:g.157201003A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201003A>T , CM000668.2:g.157201003A>T	GRCh38
NC_000006.11:g.157522137A>T , CM000668.1:g.157522137A>T	GRCh37
NC_000006.10:g.157563829A>T	NCBI36
NG_032093.1:g.428074A>T
NG_032093.2:g.428074A>T
NG_066624.1:g.429978A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4619A>T	ENSP00000055163.8:p.Asp1540Val
ENST00000414678.8:c.4688A>T	ENSP00000412835.3:p.Asp1563Val
ENST00000637015.2:c.4907A>T	ENSP00000489729.2:p.Asp1636Val
ENST00000346085.10:c.4658A>T	ENSP00000344546.5:p.Asp1553Val
ENST00000350026.10:c.4370A>T	ENSP00000055163.7:p.Asp1457Val
ENST00000414678.7:c.2936A>T	ENSP00000412835.2:p.Asp979Val
ENST00000635849.1:c.2099A>T	ENSP00000490948.1:p.Asp700Val
ENST00000635957.1:c.1730A>T	ENSP00000490385.1:p.Asp577Val
ENST00000636227.1:n.3241A>T
ENST00000636254.1:n.698A>T
ENST00000636930.2:c.4778A>T MANE Select	ENSP00000490491.2:p.Asp1593Val
ENST00000636940.1:n.2775A>T
ENST00000637015.1:c.2146A>T
ENST00000637568.1:c.2060A>T
ENST00000637741.1:n.1444A>T
ENST00000637810.1:c.2120A>T	ENSP00000489636.1:p.Asp707Val
ENST00000637904.1:c.2279A>T	ENSP00000490550.1:p.Asp760Val
ENST00000647938.1:c.4409A>T	ENSP00000498155.1:p.Asp1470Val
ENST00000346085.9:c.4409A>T	ENSP00000344546.4:p.Asp1470Val
ENST00000350026.9:c.4370A>T	ENSP00000055163.7:p.Asp1457Val
ENST00000414678.6:c.2936A>T	ENSP00000412835.2:p.Asp979Val
NM_017519.2:c.4370A>T	NP_059989.2:p.Asp1457Val
NM_020732.3:c.4409A>T	NP_065783.3:p.Asp1470Val
XM_005267069.3:c.4529A>T	XP_005267126.2:p.Asp1510Val
XM_011535984.1:c.3608A>T	XP_011534286.1:p.Asp1203Val
XM_011535985.1:c.3428A>T	XP_011534287.1:p.Asp1143Val
XM_011535986.1:c.3188A>T	XP_011534288.1:p.Asp1063Val
XM_011535987.1:c.2807A>T	XP_011534289.1:p.Asp936Val
XM_011535988.1:c.1670A>T	XP_011534290.1:p.Asp557Val
NM_001346813.1:c.4529A>T	NP_001333742.1:p.Asp1510Val
NM_001363725.1:c.2279A>T	NP_001350654.1:p.Asp760Val
XM_011535984.2:c.4739A>T	XP_011534286.2:p.Asp1580Val
XM_011535988.3:c.1670A>T	XP_011534290.1:p.Asp557Val
XM_017011103.2:c.4640A>T	XP_016866592.1:p.Asp1547Val
XM_017011104.1:c.4610A>T	XP_016866593.1:p.Asp1537Val
XM_017011105.2:c.4580A>T	XP_016866594.1:p.Asp1527Val
XM_017011106.2:c.4451A>T	XP_016866595.1:p.Asp1484Val
XM_017011107.2:c.4430A>T	XP_016866596.1:p.Asp1477Val
XR_002956289.1:n.4725A>T
NM_001363725.2:c.2279A>T	NP_001350654.1:p.Asp760Val
NM_001371656.1:c.4658A>T	NP_001358585.1:p.Asp1553Val
NM_001374820.1:c.4658A>T	NP_001361749.1:p.Asp1553Val
NM_001374828.1:c.4778A>T MANE Select	NP_001361757.1:p.Asp1593Val
NM_017519.3:c.4619A>T	NP_059989.3:p.Asp1540Val