Canonical Allele Identifier: CA366234976

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511212A>T (hg19) ; chr6:g.157190078A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190078A>T , CM000668.2:g.157190078A>T	GRCh38
NC_000006.11:g.157511212A>T , CM000668.1:g.157511212A>T	GRCh37
NC_000006.10:g.157552904A>T	NCBI36
NG_032093.1:g.417149A>T
NG_032093.2:g.417149A>T
NG_066624.1:g.419053A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3940A>T	ENSP00000055163.8:p.Ser1314Cys
ENST00000414678.8:c.4009A>T	ENSP00000412835.3:p.Ser1337Cys
ENST00000637015.2:c.4228A>T	ENSP00000489729.2:p.Ser1410Cys
ENST00000346085.10:c.3979A>T	ENSP00000344546.5:p.Ser1327Cys
ENST00000350026.10:c.3691A>T	ENSP00000055163.7:p.Ser1231Cys
ENST00000414678.7:c.2257A>T	ENSP00000412835.2:p.Ser753Cys
ENST00000635849.1:c.1420A>T	ENSP00000490948.1:p.Ser474Cys
ENST00000635957.1:c.1051A>T	ENSP00000490385.1:p.Ser351Cys
ENST00000636930.2:c.4099A>T MANE Select	ENSP00000490491.2:p.Ser1367Cys
ENST00000636940.1:n.2096A>T
ENST00000637015.1:c.1467A>T
ENST00000637568.1:c.1381A>T
ENST00000637741.1:n.765A>T
ENST00000637810.1:c.1441A>T	ENSP00000489636.1:p.Ser481Cys
ENST00000637904.1:c.1600A>T	ENSP00000490550.1:p.Ser534Cys
ENST00000647938.1:c.3730A>T	ENSP00000498155.1:p.Ser1244Cys
ENST00000346085.9:c.3730A>T	ENSP00000344546.4:p.Ser1244Cys
ENST00000350026.9:c.3691A>T	ENSP00000055163.7:p.Ser1231Cys
ENST00000414678.6:c.2257A>T	ENSP00000412835.2:p.Ser753Cys
NM_017519.2:c.3691A>T	NP_059989.2:p.Ser1231Cys
NM_020732.3:c.3730A>T	NP_065783.3:p.Ser1244Cys
XM_005267069.3:c.3850A>T	XP_005267126.2:p.Ser1284Cys
XM_011535984.1:c.2929A>T	XP_011534286.1:p.Ser977Cys
XM_011535985.1:c.2749A>T	XP_011534287.1:p.Ser917Cys
XM_011535986.1:c.2509A>T	XP_011534288.1:p.Ser837Cys
XM_011535987.1:c.2128A>T	XP_011534289.1:p.Ser710Cys
XM_011535988.1:c.991A>T	XP_011534290.1:p.Ser331Cys
NM_001346813.1:c.3850A>T	NP_001333742.1:p.Ser1284Cys
NM_001363725.1:c.1600A>T	NP_001350654.1:p.Ser534Cys
XM_011535984.2:c.4060A>T	XP_011534286.2:p.Ser1354Cys
XM_011535988.3:c.991A>T	XP_011534290.1:p.Ser331Cys
XM_017011103.2:c.3961A>T	XP_016866592.1:p.Ser1321Cys
XM_017011104.1:c.3931A>T	XP_016866593.1:p.Ser1311Cys
XM_017011105.2:c.3901A>T	XP_016866594.1:p.Ser1301Cys
XM_017011106.2:c.3772A>T	XP_016866595.1:p.Ser1258Cys
XM_017011107.2:c.3751A>T	XP_016866596.1:p.Ser1251Cys
XR_002956289.1:n.4143A>T
NM_001363725.2:c.1600A>T	NP_001350654.1:p.Ser534Cys
NM_001371656.1:c.3979A>T	NP_001358585.1:p.Ser1327Cys
NM_001374820.1:c.3979A>T	NP_001361749.1:p.Ser1327Cys
NM_001374828.1:c.4099A>T MANE Select	NP_001361757.1:p.Ser1367Cys
NM_017519.3:c.3940A>T	NP_059989.3:p.Ser1314Cys