Canonical Allele Identifier: CA366242191

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522317A>G (hg19) ; chr6:g.157201183A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201183A>G , CM000668.2:g.157201183A>G	GRCh38
NC_000006.11:g.157522317A>G , CM000668.1:g.157522317A>G	GRCh37
NC_000006.10:g.157564009A>G	NCBI36
NG_032093.1:g.428254A>G
NG_032093.2:g.428254A>G
NG_066624.1:g.430158A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4799A>G	ENSP00000055163.8:p.Gln1600Arg
ENST00000414678.8:c.4868A>G	ENSP00000412835.3:p.Gln1623Arg
ENST00000637015.2:c.5087A>G	ENSP00000489729.2:p.Gln1696Arg
ENST00000346085.10:c.4838A>G	ENSP00000344546.5:p.Gln1613Arg
ENST00000350026.10:c.4550A>G	ENSP00000055163.7:p.Gln1517Arg
ENST00000414678.7:c.3116A>G	ENSP00000412835.2:p.Gln1039Arg
ENST00000635849.1:c.2279A>G	ENSP00000490948.1:p.Gln760Arg
ENST00000635957.1:c.1910A>G	ENSP00000490385.1:p.Gln637Arg
ENST00000636227.1:n.3421A>G
ENST00000636254.1:n.878A>G
ENST00000636930.2:c.4958A>G MANE Select	ENSP00000490491.2:p.Gln1653Arg
ENST00000636940.1:n.2955A>G
ENST00000637015.1:c.2326A>G
ENST00000637568.1:c.2240A>G
ENST00000637741.1:n.1624A>G
ENST00000637810.1:c.2300A>G	ENSP00000489636.1:p.Gln767Arg
ENST00000637904.1:c.2459A>G	ENSP00000490550.1:p.Gln820Arg
ENST00000647938.1:c.4589A>G	ENSP00000498155.1:p.Gln1530Arg
ENST00000346085.9:c.4589A>G	ENSP00000344546.4:p.Gln1530Arg
ENST00000350026.9:c.4550A>G	ENSP00000055163.7:p.Gln1517Arg
ENST00000414678.6:c.3116A>G	ENSP00000412835.2:p.Gln1039Arg
NM_017519.2:c.4550A>G	NP_059989.2:p.Gln1517Arg
NM_020732.3:c.4589A>G	NP_065783.3:p.Gln1530Arg
XM_005267069.3:c.4709A>G	XP_005267126.2:p.Gln1570Arg
XM_011535984.1:c.3788A>G	XP_011534286.1:p.Gln1263Arg
XM_011535985.1:c.3608A>G	XP_011534287.1:p.Gln1203Arg
XM_011535986.1:c.3368A>G	XP_011534288.1:p.Gln1123Arg
XM_011535987.1:c.2987A>G	XP_011534289.1:p.Gln996Arg
XM_011535988.1:c.1850A>G	XP_011534290.1:p.Gln617Arg
NM_001346813.1:c.4709A>G	NP_001333742.1:p.Gln1570Arg
NM_001363725.1:c.2459A>G	NP_001350654.1:p.Gln820Arg
XM_011535984.2:c.4919A>G	XP_011534286.2:p.Gln1640Arg
XM_011535988.3:c.1850A>G	XP_011534290.1:p.Gln617Arg
XM_017011103.2:c.4820A>G	XP_016866592.1:p.Gln1607Arg
XM_017011104.1:c.4790A>G	XP_016866593.1:p.Gln1597Arg
XM_017011105.2:c.4760A>G	XP_016866594.1:p.Gln1587Arg
XM_017011106.2:c.4631A>G	XP_016866595.1:p.Gln1544Arg
XM_017011107.2:c.4610A>G	XP_016866596.1:p.Gln1537Arg
XR_002956289.1:n.4905A>G
NM_001363725.2:c.2459A>G	NP_001350654.1:p.Gln820Arg
NM_001371656.1:c.4838A>G	NP_001358585.1:p.Gln1613Arg
NM_001374820.1:c.4838A>G	NP_001361749.1:p.Gln1613Arg
NM_001374828.1:c.4958A>G MANE Select	NP_001361757.1:p.Gln1653Arg
NM_017519.3:c.4799A>G	NP_059989.3:p.Gln1600Arg