Canonical Allele Identifier: CA452781566

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510888C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189754C>G , CM000668.2:g.157189754C>G	GRCh38
NC_000006.11:g.157510888C>G , CM000668.1:g.157510888C>G	GRCh37
NC_000006.10:g.157552580C>G	NCBI36
NG_032093.1:g.416825C>G
NG_032093.2:g.416825C>G
NG_066624.1:g.418729C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3873C>G	ENSP00000055163.8:p.Gly1291=
ENST00000414678.8:c.3942C>G	ENSP00000412835.3:p.Gly1314=
ENST00000637015.2:c.4161C>G	ENSP00000489729.2:p.Gly1387=
ENST00000346085.10:c.3912C>G	ENSP00000344546.5:p.Gly1304=
ENST00000350026.10:c.3624C>G	ENSP00000055163.7:p.Gly1208=
ENST00000414678.7:c.2190C>G	ENSP00000412835.2:p.Gly730=
ENST00000635849.1:c.1353C>G	ENSP00000490948.1:p.Gly451=
ENST00000635957.1:c.987C>G	ENSP00000490385.1:p.Gly329=
ENST00000636930.2:c.4032C>G MANE Select	ENSP00000490491.2:p.Gly1344=
ENST00000636940.1:n.2029C>G
ENST00000637015.1:c.1400C>G
ENST00000637568.1:c.1314C>G
ENST00000637741.1:n.698C>G
ENST00000637810.1:c.1374C>G	ENSP00000489636.1:p.Gly458=
ENST00000637904.1:c.1533C>G	ENSP00000490550.1:p.Gly511=
ENST00000647938.1:c.3663C>G	ENSP00000498155.1:p.Gly1221=
ENST00000346085.9:c.3663C>G	ENSP00000344546.4:p.Gly1221=
ENST00000350026.9:c.3624C>G	ENSP00000055163.7:p.Gly1208=
ENST00000414678.6:c.2190C>G	ENSP00000412835.2:p.Gly730=
NM_017519.2:c.3624C>G	NP_059989.2:p.Gly1208=
NM_020732.3:c.3663C>G	NP_065783.3:p.Gly1221=
XM_005267069.3:c.3783C>G	XP_005267126.2:p.Gly1261=
XM_011535984.1:c.2862C>G	XP_011534286.1:p.Gly954=
XM_011535985.1:c.2682C>G	XP_011534287.1:p.Gly894=
XM_011535986.1:c.2442C>G	XP_011534288.1:p.Gly814=
XM_011535987.1:c.2061C>G	XP_011534289.1:p.Gly687=
XM_011535988.1:c.924C>G	XP_011534290.1:p.Gly308=
NM_001346813.1:c.3783C>G	NP_001333742.1:p.Gly1261=
NM_001363725.1:c.1533C>G	NP_001350654.1:p.Gly511=
XM_011535984.2:c.3993C>G	XP_011534286.2:p.Gly1331=
XM_011535988.3:c.924C>G	XP_011534290.1:p.Gly308=
XM_017011103.2:c.3894C>G	XP_016866592.1:p.Gly1298=
XM_017011104.1:c.3864C>G	XP_016866593.1:p.Gly1288=
XM_017011105.2:c.3834C>G	XP_016866594.1:p.Gly1278=
XM_017011106.2:c.3705C>G	XP_016866595.1:p.Gly1235=
XM_017011107.2:c.3684C>G	XP_016866596.1:p.Gly1228=
XR_002956289.1:n.4076C>G
NM_001363725.2:c.1533C>G	NP_001350654.1:p.Gly511=
NM_001371656.1:c.3912C>G	NP_001358585.1:p.Gly1304=
NM_001374820.1:c.3912C>G	NP_001361749.1:p.Gly1304=
NM_001374828.1:c.4032C>G MANE Select	NP_001361757.1:p.Gly1344=
NM_017519.3:c.3873C>G	NP_059989.3:p.Gly1291=