Canonical Allele Identifier: CA366235315

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511255C>T (hg19) ; chr6:g.157190121C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190121C>T , CM000668.2:g.157190121C>T	GRCh38
NC_000006.11:g.157511255C>T , CM000668.1:g.157511255C>T	GRCh37
NC_000006.10:g.157552947C>T	NCBI36
NG_032093.1:g.417192C>T
NG_032093.2:g.417192C>T
NG_066624.1:g.419096C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3983C>T	ENSP00000055163.8:p.Ala1328Val
ENST00000414678.8:c.4052C>T	ENSP00000412835.3:p.Ala1351Val
ENST00000637015.2:c.4271C>T	ENSP00000489729.2:p.Ala1424Val
ENST00000346085.10:c.4022C>T	ENSP00000344546.5:p.Ala1341Val
ENST00000350026.10:c.3734C>T	ENSP00000055163.7:p.Ala1245Val
ENST00000414678.7:c.2300C>T	ENSP00000412835.2:p.Ala767Val
ENST00000635849.1:c.1463C>T	ENSP00000490948.1:p.Ala488Val
ENST00000635957.1:c.1094C>T	ENSP00000490385.1:p.Ala365Val
ENST00000636930.2:c.4142C>T MANE Select	ENSP00000490491.2:p.Ala1381Val
ENST00000636940.1:n.2139C>T
ENST00000637015.1:c.1510C>T
ENST00000637568.1:c.1424C>T
ENST00000637741.1:n.808C>T
ENST00000637810.1:c.1484C>T	ENSP00000489636.1:p.Ala495Val
ENST00000637904.1:c.1643C>T	ENSP00000490550.1:p.Ala548Val
ENST00000647938.1:c.3773C>T	ENSP00000498155.1:p.Ala1258Val
ENST00000346085.9:c.3773C>T	ENSP00000344546.4:p.Ala1258Val
ENST00000350026.9:c.3734C>T	ENSP00000055163.7:p.Ala1245Val
ENST00000414678.6:c.2300C>T	ENSP00000412835.2:p.Ala767Val
NM_017519.2:c.3734C>T	NP_059989.2:p.Ala1245Val
NM_020732.3:c.3773C>T	NP_065783.3:p.Ala1258Val
XM_005267069.3:c.3893C>T	XP_005267126.2:p.Ala1298Val
XM_011535984.1:c.2972C>T	XP_011534286.1:p.Ala991Val
XM_011535985.1:c.2792C>T	XP_011534287.1:p.Ala931Val
XM_011535986.1:c.2552C>T	XP_011534288.1:p.Ala851Val
XM_011535987.1:c.2171C>T	XP_011534289.1:p.Ala724Val
XM_011535988.1:c.1034C>T	XP_011534290.1:p.Ala345Val
NM_001346813.1:c.3893C>T	NP_001333742.1:p.Ala1298Val
NM_001363725.1:c.1643C>T	NP_001350654.1:p.Ala548Val
XM_011535984.2:c.4103C>T	XP_011534286.2:p.Ala1368Val
XM_011535988.3:c.1034C>T	XP_011534290.1:p.Ala345Val
XM_017011103.2:c.4004C>T	XP_016866592.1:p.Ala1335Val
XM_017011104.1:c.3974C>T	XP_016866593.1:p.Ala1325Val
XM_017011105.2:c.3944C>T	XP_016866594.1:p.Ala1315Val
XM_017011106.2:c.3815C>T	XP_016866595.1:p.Ala1272Val
XM_017011107.2:c.3794C>T	XP_016866596.1:p.Ala1265Val
XR_002956289.1:n.4186C>T
NM_001363725.2:c.1643C>T	NP_001350654.1:p.Ala548Val
NM_001371656.1:c.4022C>T	NP_001358585.1:p.Ala1341Val
NM_001374820.1:c.4022C>T	NP_001361749.1:p.Ala1341Val
NM_001374828.1:c.4142C>T MANE Select	NP_001361757.1:p.Ala1381Val
NM_017519.3:c.3983C>T	NP_059989.3:p.Ala1328Val