Canonical Allele Identifier: CA366381014

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157222658A>G (hg19) ; chr6:g.156901524A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901524A>G , CM000668.2:g.156901524A>G	GRCh38
NC_000006.11:g.157222658A>G , CM000668.1:g.157222658A>G	GRCh37
NC_000006.10:g.157264350A>G	NCBI36
NG_032093.1:g.128595A>G
NG_032093.2:g.128595A>G
NG_066624.1:g.130499A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2135A>G	ENSP00000055163.8:p.Gln712Arg
ENST00000414678.8:c.2135A>G	ENSP00000412835.3:p.Gln712Arg
ENST00000637015.2:c.2135A>G	ENSP00000489729.2:p.Gln712Arg
ENST00000319584.11:c.149A>G	ENSP00000313006.7:p.Gln50Arg
ENST00000346085.10:c.2174A>G	ENSP00000344546.5:p.Gln725Arg
ENST00000350026.10:c.1886A>G	ENSP00000055163.7:p.Gln629Arg
ENST00000414678.7:c.383A>G	ENSP00000412835.2:p.Gln128Arg
ENST00000636205.1:n.198A>G
ENST00000636748.1:c.416A>G	ENSP00000489917.1:p.Gln139Arg
ENST00000636930.2:c.2135A>G MANE Select	ENSP00000490491.2:p.Gln712Arg
ENST00000637532.1:c.161A>G	ENSP00000490420.1:p.Gln54Arg
ENST00000638000.1:c.352A>G
ENST00000647938.1:c.1925A>G	ENSP00000498155.1:p.Gln642Arg
ENST00000674190.1:n.842A>G
ENST00000674298.1:c.1875A>G
ENST00000319584.10:c.152A>G	ENSP00000313006.6:p.Gln51Arg
ENST00000346085.9:c.1925A>G	ENSP00000344546.4:p.Gln642Arg
ENST00000350026.9:c.1886A>G	ENSP00000055163.7:p.Gln629Arg
ENST00000414678.6:c.383A>G	ENSP00000412835.2:p.Gln128Arg
NM_017519.2:c.1886A>G	NP_059989.2:p.Gln629Arg
NM_020732.3:c.1925A>G	NP_065783.3:p.Gln642Arg
XM_005267069.3:c.1886A>G	XP_005267126.2:p.Gln629Arg
XM_011535984.1:c.794A>G	XP_011534286.1:p.Gln265Arg
XM_011535985.1:c.794A>G	XP_011534287.1:p.Gln265Arg
XM_011535986.1:c.374A>G	XP_011534288.1:p.Gln125Arg
NM_001346813.1:c.1886A>G	NP_001333742.1:p.Gln629Arg
XM_011535984.2:c.1925A>G	XP_011534286.2:p.Gln642Arg
XM_017011103.2:c.1925A>G	XP_016866592.1:p.Gln642Arg
XM_017011104.1:c.1925A>G	XP_016866593.1:p.Gln642Arg
XM_017011105.2:c.1925A>G	XP_016866594.1:p.Gln642Arg
XM_017011106.2:c.1925A>G	XP_016866595.1:p.Gln642Arg
XM_017011107.2:c.1925A>G	XP_016866596.1:p.Gln642Arg
XR_002956289.1:n.2008A>G
NM_001371656.1:c.2174A>G	NP_001358585.1:p.Gln725Arg
NM_001374820.1:c.2174A>G	NP_001361749.1:p.Gln725Arg
NM_001374828.1:c.2135A>G MANE Select	NP_001361757.1:p.Gln712Arg
NM_017519.3:c.2135A>G	NP_059989.3:p.Gln712Arg