Canonical Allele Identifier: CA366234595

Gene: ARID1B

Linked Data

• dbSNP Id: rs369035728
• MyVariant Identifiers: chr6:g.157511175C>A (hg19) ; chr6:g.157190041C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190041C>A , CM000668.2:g.157190041C>A	GRCh38
NC_000006.11:g.157511175C>A , CM000668.1:g.157511175C>A	GRCh37
NC_000006.10:g.157552867C>A	NCBI36
NG_032093.1:g.417112C>A
NG_032093.2:g.417112C>A
NG_066624.1:g.419016C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3903C>A	ENSP00000055163.8:p.Ser1301Arg
ENST00000414678.8:c.3972C>A	ENSP00000412835.3:p.Ser1324Arg
ENST00000637015.2:c.4191C>A	ENSP00000489729.2:p.Ser1397Arg
ENST00000346085.10:c.3942C>A	ENSP00000344546.5:p.Ser1314Arg
ENST00000350026.10:c.3654C>A	ENSP00000055163.7:p.Ser1218Arg
ENST00000414678.7:c.2220C>A	ENSP00000412835.2:p.Ser740Arg
ENST00000635849.1:c.1383C>A	ENSP00000490948.1:p.Ser461Arg
ENST00000635957.1:c.1014C>A	ENSP00000490385.1:p.Ser338Arg
ENST00000636930.2:c.4062C>A MANE Select	ENSP00000490491.2:p.Ser1354Arg
ENST00000636940.1:n.2059C>A
ENST00000637015.1:c.1430C>A
ENST00000637568.1:c.1344C>A
ENST00000637741.1:n.728C>A
ENST00000637810.1:c.1404C>A	ENSP00000489636.1:p.Ser468Arg
ENST00000637904.1:c.1563C>A	ENSP00000490550.1:p.Ser521Arg
ENST00000647938.1:c.3693C>A	ENSP00000498155.1:p.Ser1231Arg
ENST00000346085.9:c.3693C>A	ENSP00000344546.4:p.Ser1231Arg
ENST00000350026.9:c.3654C>A	ENSP00000055163.7:p.Ser1218Arg
ENST00000414678.6:c.2220C>A	ENSP00000412835.2:p.Ser740Arg
NM_017519.2:c.3654C>A	NP_059989.2:p.Ser1218Arg
NM_020732.3:c.3693C>A	NP_065783.3:p.Ser1231Arg
XM_005267069.3:c.3813C>A	XP_005267126.2:p.Ser1271Arg
XM_011535984.1:c.2892C>A	XP_011534286.1:p.Ser964Arg
XM_011535985.1:c.2712C>A	XP_011534287.1:p.Ser904Arg
XM_011535986.1:c.2472C>A	XP_011534288.1:p.Ser824Arg
XM_011535987.1:c.2091C>A	XP_011534289.1:p.Ser697Arg
XM_011535988.1:c.954C>A	XP_011534290.1:p.Ser318Arg
NM_001346813.1:c.3813C>A	NP_001333742.1:p.Ser1271Arg
NM_001363725.1:c.1563C>A	NP_001350654.1:p.Ser521Arg
XM_011535984.2:c.4023C>A	XP_011534286.2:p.Ser1341Arg
XM_011535988.3:c.954C>A	XP_011534290.1:p.Ser318Arg
XM_017011103.2:c.3924C>A	XP_016866592.1:p.Ser1308Arg
XM_017011104.1:c.3894C>A	XP_016866593.1:p.Ser1298Arg
XM_017011105.2:c.3864C>A	XP_016866594.1:p.Ser1288Arg
XM_017011106.2:c.3735C>A	XP_016866595.1:p.Ser1245Arg
XM_017011107.2:c.3714C>A	XP_016866596.1:p.Ser1238Arg
XR_002956289.1:n.4106C>A
NM_001363725.2:c.1563C>A	NP_001350654.1:p.Ser521Arg
NM_001371656.1:c.3942C>A	NP_001358585.1:p.Ser1314Arg
NM_001374820.1:c.3942C>A	NP_001361749.1:p.Ser1314Arg
NM_001374828.1:c.4062C>A MANE Select	NP_001361757.1:p.Ser1354Arg
NM_017519.3:c.3903C>A	NP_059989.3:p.Ser1301Arg