Canonical Allele Identifier: CA452978389

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522174C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201040C>G , CM000668.2:g.157201040C>G	GRCh38
NC_000006.11:g.157522174C>G , CM000668.1:g.157522174C>G	GRCh37
NC_000006.10:g.157563866C>G	NCBI36
NG_032093.1:g.428111C>G
NG_032093.2:g.428111C>G
NG_066624.1:g.430015C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4656C>G	ENSP00000055163.8:p.Gly1552=
ENST00000414678.8:c.4725C>G	ENSP00000412835.3:p.Gly1575=
ENST00000637015.2:c.4944C>G	ENSP00000489729.2:p.Gly1648=
ENST00000346085.10:c.4695C>G	ENSP00000344546.5:p.Gly1565=
ENST00000350026.10:c.4407C>G	ENSP00000055163.7:p.Gly1469=
ENST00000414678.7:c.2973C>G	ENSP00000412835.2:p.Gly991=
ENST00000635849.1:c.2136C>G	ENSP00000490948.1:p.Gly712=
ENST00000635957.1:c.1767C>G	ENSP00000490385.1:p.Gly589=
ENST00000636227.1:n.3278C>G
ENST00000636254.1:n.735C>G
ENST00000636930.2:c.4815C>G MANE Select	ENSP00000490491.2:p.Gly1605=
ENST00000636940.1:n.2812C>G
ENST00000637015.1:c.2183C>G
ENST00000637568.1:c.2097C>G
ENST00000637741.1:n.1481C>G
ENST00000637810.1:c.2157C>G	ENSP00000489636.1:p.Gly719=
ENST00000637904.1:c.2316C>G	ENSP00000490550.1:p.Gly772=
ENST00000647938.1:c.4446C>G	ENSP00000498155.1:p.Gly1482=
ENST00000346085.9:c.4446C>G	ENSP00000344546.4:p.Gly1482=
ENST00000350026.9:c.4407C>G	ENSP00000055163.7:p.Gly1469=
ENST00000414678.6:c.2973C>G	ENSP00000412835.2:p.Gly991=
NM_017519.2:c.4407C>G	NP_059989.2:p.Gly1469=
NM_020732.3:c.4446C>G	NP_065783.3:p.Gly1482=
XM_005267069.3:c.4566C>G	XP_005267126.2:p.Gly1522=
XM_011535984.1:c.3645C>G	XP_011534286.1:p.Gly1215=
XM_011535985.1:c.3465C>G	XP_011534287.1:p.Gly1155=
XM_011535986.1:c.3225C>G	XP_011534288.1:p.Gly1075=
XM_011535987.1:c.2844C>G	XP_011534289.1:p.Gly948=
XM_011535988.1:c.1707C>G	XP_011534290.1:p.Gly569=
NM_001346813.1:c.4566C>G	NP_001333742.1:p.Gly1522=
NM_001363725.1:c.2316C>G	NP_001350654.1:p.Gly772=
XM_011535984.2:c.4776C>G	XP_011534286.2:p.Gly1592=
XM_011535988.3:c.1707C>G	XP_011534290.1:p.Gly569=
XM_017011103.2:c.4677C>G	XP_016866592.1:p.Gly1559=
XM_017011104.1:c.4647C>G	XP_016866593.1:p.Gly1549=
XM_017011105.2:c.4617C>G	XP_016866594.1:p.Gly1539=
XM_017011106.2:c.4488C>G	XP_016866595.1:p.Gly1496=
XM_017011107.2:c.4467C>G	XP_016866596.1:p.Gly1489=
XR_002956289.1:n.4762C>G
NM_001363725.2:c.2316C>G	NP_001350654.1:p.Gly772=
NM_001371656.1:c.4695C>G	NP_001358585.1:p.Gly1565=
NM_001374820.1:c.4695C>G	NP_001361749.1:p.Gly1565=
NM_001374828.1:c.4815C>G MANE Select	NP_001361757.1:p.Gly1605=
NM_017519.3:c.4656C>G	NP_059989.3:p.Gly1552=