Canonical Allele Identifier: CA366242002

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522237T>A (hg19) ; chr6:g.157201103T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201103T>A , CM000668.2:g.157201103T>A	GRCh38
NC_000006.11:g.157522237T>A , CM000668.1:g.157522237T>A	GRCh37
NC_000006.10:g.157563929T>A	NCBI36
NG_032093.1:g.428174T>A
NG_032093.2:g.428174T>A
NG_066624.1:g.430078T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4719T>A	ENSP00000055163.8:p.Asp1573Glu
ENST00000414678.8:c.4788T>A	ENSP00000412835.3:p.Asp1596Glu
ENST00000637015.2:c.5007T>A	ENSP00000489729.2:p.Asp1669Glu
ENST00000346085.10:c.4758T>A	ENSP00000344546.5:p.Asp1586Glu
ENST00000350026.10:c.4470T>A	ENSP00000055163.7:p.Asp1490Glu
ENST00000414678.7:c.3036T>A	ENSP00000412835.2:p.Asp1012Glu
ENST00000635849.1:c.2199T>A	ENSP00000490948.1:p.Asp733Glu
ENST00000635957.1:c.1830T>A	ENSP00000490385.1:p.Asp610Glu
ENST00000636227.1:n.3341T>A
ENST00000636254.1:n.798T>A
ENST00000636930.2:c.4878T>A MANE Select	ENSP00000490491.2:p.Asp1626Glu
ENST00000636940.1:n.2875T>A
ENST00000637015.1:c.2246T>A
ENST00000637568.1:c.2160T>A
ENST00000637741.1:n.1544T>A
ENST00000637810.1:c.2220T>A	ENSP00000489636.1:p.Asp740Glu
ENST00000637904.1:c.2379T>A	ENSP00000490550.1:p.Asp793Glu
ENST00000647938.1:c.4509T>A	ENSP00000498155.1:p.Asp1503Glu
ENST00000346085.9:c.4509T>A	ENSP00000344546.4:p.Asp1503Glu
ENST00000350026.9:c.4470T>A	ENSP00000055163.7:p.Asp1490Glu
ENST00000414678.6:c.3036T>A	ENSP00000412835.2:p.Asp1012Glu
NM_017519.2:c.4470T>A	NP_059989.2:p.Asp1490Glu
NM_020732.3:c.4509T>A	NP_065783.3:p.Asp1503Glu
XM_005267069.3:c.4629T>A	XP_005267126.2:p.Asp1543Glu
XM_011535984.1:c.3708T>A	XP_011534286.1:p.Asp1236Glu
XM_011535985.1:c.3528T>A	XP_011534287.1:p.Asp1176Glu
XM_011535986.1:c.3288T>A	XP_011534288.1:p.Asp1096Glu
XM_011535987.1:c.2907T>A	XP_011534289.1:p.Asp969Glu
XM_011535988.1:c.1770T>A	XP_011534290.1:p.Asp590Glu
NM_001346813.1:c.4629T>A	NP_001333742.1:p.Asp1543Glu
NM_001363725.1:c.2379T>A	NP_001350654.1:p.Asp793Glu
XM_011535984.2:c.4839T>A	XP_011534286.2:p.Asp1613Glu
XM_011535988.3:c.1770T>A	XP_011534290.1:p.Asp590Glu
XM_017011103.2:c.4740T>A	XP_016866592.1:p.Asp1580Glu
XM_017011104.1:c.4710T>A	XP_016866593.1:p.Asp1570Glu
XM_017011105.2:c.4680T>A	XP_016866594.1:p.Asp1560Glu
XM_017011106.2:c.4551T>A	XP_016866595.1:p.Asp1517Glu
XM_017011107.2:c.4530T>A	XP_016866596.1:p.Asp1510Glu
XR_002956289.1:n.4825T>A
NM_001363725.2:c.2379T>A	NP_001350654.1:p.Asp793Glu
NM_001371656.1:c.4758T>A	NP_001358585.1:p.Asp1586Glu
NM_001374820.1:c.4758T>A	NP_001361749.1:p.Asp1586Glu
NM_001374828.1:c.4878T>A MANE Select	NP_001361757.1:p.Asp1626Glu
NM_017519.3:c.4719T>A	NP_059989.3:p.Asp1573Glu