Canonical Allele Identifier: CA366241390

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522125C>T (hg19) ; chr6:g.157200991C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200991C>T , CM000668.2:g.157200991C>T	GRCh38
NC_000006.11:g.157522125C>T , CM000668.1:g.157522125C>T	GRCh37
NC_000006.10:g.157563817C>T	NCBI36
NG_032093.1:g.428062C>T
NG_032093.2:g.428062C>T
NG_066624.1:g.429966C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4607C>T	ENSP00000055163.8:p.Ala1536Val
ENST00000414678.8:c.4676C>T	ENSP00000412835.3:p.Ala1559Val
ENST00000637015.2:c.4895C>T	ENSP00000489729.2:p.Ala1632Val
ENST00000346085.10:c.4646C>T	ENSP00000344546.5:p.Ala1549Val
ENST00000350026.10:c.4358C>T	ENSP00000055163.7:p.Ala1453Val
ENST00000414678.7:c.2924C>T	ENSP00000412835.2:p.Ala975Val
ENST00000635849.1:c.2087C>T	ENSP00000490948.1:p.Ala696Val
ENST00000635957.1:c.1718C>T	ENSP00000490385.1:p.Ala573Val
ENST00000636227.1:n.3229C>T
ENST00000636254.1:n.686C>T
ENST00000636930.2:c.4766C>T MANE Select	ENSP00000490491.2:p.Ala1589Val
ENST00000636940.1:n.2763C>T
ENST00000637015.1:c.2134C>T
ENST00000637568.1:c.2048C>T
ENST00000637741.1:n.1432C>T
ENST00000637810.1:c.2108C>T	ENSP00000489636.1:p.Ala703Val
ENST00000637904.1:c.2267C>T	ENSP00000490550.1:p.Ala756Val
ENST00000647938.1:c.4397C>T	ENSP00000498155.1:p.Ala1466Val
ENST00000346085.9:c.4397C>T	ENSP00000344546.4:p.Ala1466Val
ENST00000350026.9:c.4358C>T	ENSP00000055163.7:p.Ala1453Val
ENST00000414678.6:c.2924C>T	ENSP00000412835.2:p.Ala975Val
NM_017519.2:c.4358C>T	NP_059989.2:p.Ala1453Val
NM_020732.3:c.4397C>T	NP_065783.3:p.Ala1466Val
XM_005267069.3:c.4517C>T	XP_005267126.2:p.Ala1506Val
XM_011535984.1:c.3596C>T	XP_011534286.1:p.Ala1199Val
XM_011535985.1:c.3416C>T	XP_011534287.1:p.Ala1139Val
XM_011535986.1:c.3176C>T	XP_011534288.1:p.Ala1059Val
XM_011535987.1:c.2795C>T	XP_011534289.1:p.Ala932Val
XM_011535988.1:c.1658C>T	XP_011534290.1:p.Ala553Val
NM_001346813.1:c.4517C>T	NP_001333742.1:p.Ala1506Val
NM_001363725.1:c.2267C>T	NP_001350654.1:p.Ala756Val
XM_011535984.2:c.4727C>T	XP_011534286.2:p.Ala1576Val
XM_011535988.3:c.1658C>T	XP_011534290.1:p.Ala553Val
XM_017011103.2:c.4628C>T	XP_016866592.1:p.Ala1543Val
XM_017011104.1:c.4598C>T	XP_016866593.1:p.Ala1533Val
XM_017011105.2:c.4568C>T	XP_016866594.1:p.Ala1523Val
XM_017011106.2:c.4439C>T	XP_016866595.1:p.Ala1480Val
XM_017011107.2:c.4418C>T	XP_016866596.1:p.Ala1473Val
XR_002956289.1:n.4713C>T
NM_001363725.2:c.2267C>T	NP_001350654.1:p.Ala756Val
NM_001371656.1:c.4646C>T	NP_001358585.1:p.Ala1549Val
NM_001374820.1:c.4646C>T	NP_001361749.1:p.Ala1549Val
NM_001374828.1:c.4766C>T MANE Select	NP_001361757.1:p.Ala1589Val
NM_017519.3:c.4607C>T	NP_059989.3:p.Ala1536Val