Canonical Allele Identifier: CA452978312

Gene: ARID1B

Linked Data

• dbSNP Id: rs1794065448
• MyVariant Identifiers: chr6:g.157522126A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200992A>G , CM000668.2:g.157200992A>G	GRCh38
NC_000006.11:g.157522126A>G , CM000668.1:g.157522126A>G	GRCh37
NC_000006.10:g.157563818A>G	NCBI36
NG_032093.1:g.428063A>G
NG_032093.2:g.428063A>G
NG_066624.1:g.429967A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4608A>G	ENSP00000055163.8:p.Ala1536=
ENST00000414678.8:c.4677A>G	ENSP00000412835.3:p.Ala1559=
ENST00000637015.2:c.4896A>G	ENSP00000489729.2:p.Ala1632=
ENST00000346085.10:c.4647A>G	ENSP00000344546.5:p.Ala1549=
ENST00000350026.10:c.4359A>G	ENSP00000055163.7:p.Ala1453=
ENST00000414678.7:c.2925A>G	ENSP00000412835.2:p.Ala975=
ENST00000635849.1:c.2088A>G	ENSP00000490948.1:p.Ala696=
ENST00000635957.1:c.1719A>G	ENSP00000490385.1:p.Ala573=
ENST00000636227.1:n.3230A>G
ENST00000636254.1:n.687A>G
ENST00000636930.2:c.4767A>G MANE Select	ENSP00000490491.2:p.Ala1589=
ENST00000636940.1:n.2764A>G
ENST00000637015.1:c.2135A>G
ENST00000637568.1:c.2049A>G
ENST00000637741.1:n.1433A>G
ENST00000637810.1:c.2109A>G	ENSP00000489636.1:p.Ala703=
ENST00000637904.1:c.2268A>G	ENSP00000490550.1:p.Ala756=
ENST00000647938.1:c.4398A>G	ENSP00000498155.1:p.Ala1466=
ENST00000346085.9:c.4398A>G	ENSP00000344546.4:p.Ala1466=
ENST00000350026.9:c.4359A>G	ENSP00000055163.7:p.Ala1453=
ENST00000414678.6:c.2925A>G	ENSP00000412835.2:p.Ala975=
NM_017519.2:c.4359A>G	NP_059989.2:p.Ala1453=
NM_020732.3:c.4398A>G	NP_065783.3:p.Ala1466=
XM_005267069.3:c.4518A>G	XP_005267126.2:p.Ala1506=
XM_011535984.1:c.3597A>G	XP_011534286.1:p.Ala1199=
XM_011535985.1:c.3417A>G	XP_011534287.1:p.Ala1139=
XM_011535986.1:c.3177A>G	XP_011534288.1:p.Ala1059=
XM_011535987.1:c.2796A>G	XP_011534289.1:p.Ala932=
XM_011535988.1:c.1659A>G	XP_011534290.1:p.Ala553=
NM_001346813.1:c.4518A>G	NP_001333742.1:p.Ala1506=
NM_001363725.1:c.2268A>G	NP_001350654.1:p.Ala756=
XM_011535984.2:c.4728A>G	XP_011534286.2:p.Ala1576=
XM_011535988.3:c.1659A>G	XP_011534290.1:p.Ala553=
XM_017011103.2:c.4629A>G	XP_016866592.1:p.Ala1543=
XM_017011104.1:c.4599A>G	XP_016866593.1:p.Ala1533=
XM_017011105.2:c.4569A>G	XP_016866594.1:p.Ala1523=
XM_017011106.2:c.4440A>G	XP_016866595.1:p.Ala1480=
XM_017011107.2:c.4419A>G	XP_016866596.1:p.Ala1473=
XR_002956289.1:n.4714A>G
NM_001363725.2:c.2268A>G	NP_001350654.1:p.Ala756=
NM_001371656.1:c.4647A>G	NP_001358585.1:p.Ala1549=
NM_001374820.1:c.4647A>G	NP_001361749.1:p.Ala1549=
NM_001374828.1:c.4767A>G MANE Select	NP_001361757.1:p.Ala1589=
NM_017519.3:c.4608A>G	NP_059989.3:p.Ala1536=