Canonical Allele Identifier: CA366242368

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522403T>G (hg19) ; chr6:g.157201269T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201269T>G , CM000668.2:g.157201269T>G	GRCh38
NC_000006.11:g.157522403T>G , CM000668.1:g.157522403T>G	GRCh37
NC_000006.10:g.157564095T>G	NCBI36
NG_032093.1:g.428340T>G
NG_032093.2:g.428340T>G
NG_066624.1:g.430244T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4885T>G	ENSP00000055163.8:p.Phe1629Val
ENST00000414678.8:c.4954T>G	ENSP00000412835.3:p.Phe1652Val
ENST00000637015.2:c.5173T>G	ENSP00000489729.2:p.Phe1725Val
ENST00000346085.10:c.4924T>G	ENSP00000344546.5:p.Phe1642Val
ENST00000350026.10:c.4636T>G	ENSP00000055163.7:p.Phe1546Val
ENST00000414678.7:c.3202T>G	ENSP00000412835.2:p.Phe1068Val
ENST00000635849.1:c.2365T>G	ENSP00000490948.1:p.Phe789Val
ENST00000635957.1:c.1996T>G	ENSP00000490385.1:p.Phe666Val
ENST00000636227.1:n.3507T>G
ENST00000636254.1:n.964T>G
ENST00000636930.2:c.5044T>G MANE Select	ENSP00000490491.2:p.Phe1682Val
ENST00000636940.1:n.3041T>G
ENST00000637015.1:c.2412T>G
ENST00000637568.1:c.2326T>G
ENST00000637741.1:n.1710T>G
ENST00000637810.1:c.2386T>G	ENSP00000489636.1:p.Phe796Val
ENST00000637904.1:c.2545T>G	ENSP00000490550.1:p.Phe849Val
ENST00000647938.1:c.4675T>G	ENSP00000498155.1:p.Phe1559Val
ENST00000346085.9:c.4675T>G	ENSP00000344546.4:p.Phe1559Val
ENST00000350026.9:c.4636T>G	ENSP00000055163.7:p.Phe1546Val
ENST00000414678.6:c.3202T>G	ENSP00000412835.2:p.Phe1068Val
NM_017519.2:c.4636T>G	NP_059989.2:p.Phe1546Val
NM_020732.3:c.4675T>G	NP_065783.3:p.Phe1559Val
XM_005267069.3:c.4795T>G	XP_005267126.2:p.Phe1599Val
XM_011535984.1:c.3874T>G	XP_011534286.1:p.Phe1292Val
XM_011535985.1:c.3694T>G	XP_011534287.1:p.Phe1232Val
XM_011535986.1:c.3454T>G	XP_011534288.1:p.Phe1152Val
XM_011535987.1:c.3073T>G	XP_011534289.1:p.Phe1025Val
XM_011535988.1:c.1936T>G	XP_011534290.1:p.Phe646Val
NM_001346813.1:c.4795T>G	NP_001333742.1:p.Phe1599Val
NM_001363725.1:c.2545T>G	NP_001350654.1:p.Phe849Val
XM_011535984.2:c.5005T>G	XP_011534286.2:p.Phe1669Val
XM_011535988.3:c.1936T>G	XP_011534290.1:p.Phe646Val
XM_017011103.2:c.4906T>G	XP_016866592.1:p.Phe1636Val
XM_017011104.1:c.4876T>G	XP_016866593.1:p.Phe1626Val
XM_017011105.2:c.4846T>G	XP_016866594.1:p.Phe1616Val
XM_017011106.2:c.4717T>G	XP_016866595.1:p.Phe1573Val
XM_017011107.2:c.4696T>G	XP_016866596.1:p.Phe1566Val
XR_002956289.1:n.4991T>G
NM_001363725.2:c.2545T>G	NP_001350654.1:p.Phe849Val
NM_001371656.1:c.4924T>G	NP_001358585.1:p.Phe1642Val
NM_001374820.1:c.4924T>G	NP_001361749.1:p.Phe1642Val
NM_001374828.1:c.5044T>G MANE Select	NP_001361757.1:p.Phe1682Val
NM_017519.3:c.4885T>G	NP_059989.3:p.Phe1629Val