Canonical Allele Identifier: CA452781535

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510849T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189715T>C , CM000668.2:g.157189715T>C	GRCh38
NC_000006.11:g.157510849T>C , CM000668.1:g.157510849T>C	GRCh37
NC_000006.10:g.157552541T>C	NCBI36
NG_032093.1:g.416786T>C
NG_032093.2:g.416786T>C
NG_066624.1:g.418690T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3834T>C	ENSP00000055163.8:p.Gly1278=
ENST00000414678.8:c.3903T>C	ENSP00000412835.3:p.Gly1301=
ENST00000637015.2:c.4122T>C	ENSP00000489729.2:p.Gly1374=
ENST00000346085.10:c.3873T>C	ENSP00000344546.5:p.Gly1291=
ENST00000350026.10:c.3585T>C	ENSP00000055163.7:p.Gly1195=
ENST00000414678.7:c.2151T>C	ENSP00000412835.2:p.Gly717=
ENST00000635849.1:c.1314T>C	ENSP00000490948.1:p.Gly438=
ENST00000635957.1:c.948T>C	ENSP00000490385.1:p.Gly316=
ENST00000636930.2:c.3993T>C MANE Select	ENSP00000490491.2:p.Gly1331=
ENST00000636940.1:n.1990T>C
ENST00000637015.1:c.1361T>C
ENST00000637568.1:c.1275T>C
ENST00000637741.1:n.659T>C
ENST00000637810.1:c.1335T>C	ENSP00000489636.1:p.Gly445=
ENST00000637904.1:c.1494T>C	ENSP00000490550.1:p.Gly498=
ENST00000647938.1:c.3624T>C	ENSP00000498155.1:p.Gly1208=
ENST00000346085.9:c.3624T>C	ENSP00000344546.4:p.Gly1208=
ENST00000350026.9:c.3585T>C	ENSP00000055163.7:p.Gly1195=
ENST00000414678.6:c.2151T>C	ENSP00000412835.2:p.Gly717=
NM_017519.2:c.3585T>C	NP_059989.2:p.Gly1195=
NM_020732.3:c.3624T>C	NP_065783.3:p.Gly1208=
XM_005267069.3:c.3744T>C	XP_005267126.2:p.Gly1248=
XM_011535984.1:c.2823T>C	XP_011534286.1:p.Gly941=
XM_011535985.1:c.2643T>C	XP_011534287.1:p.Gly881=
XM_011535986.1:c.2403T>C	XP_011534288.1:p.Gly801=
XM_011535987.1:c.2022T>C	XP_011534289.1:p.Gly674=
XM_011535988.1:c.885T>C	XP_011534290.1:p.Gly295=
NM_001346813.1:c.3744T>C	NP_001333742.1:p.Gly1248=
NM_001363725.1:c.1494T>C	NP_001350654.1:p.Gly498=
XM_011535984.2:c.3954T>C	XP_011534286.2:p.Gly1318=
XM_011535988.3:c.885T>C	XP_011534290.1:p.Gly295=
XM_017011103.2:c.3855T>C	XP_016866592.1:p.Gly1285=
XM_017011104.1:c.3825T>C	XP_016866593.1:p.Gly1275=
XM_017011105.2:c.3795T>C	XP_016866594.1:p.Gly1265=
XM_017011106.2:c.3666T>C	XP_016866595.1:p.Gly1222=
XM_017011107.2:c.3645T>C	XP_016866596.1:p.Gly1215=
XR_002956289.1:n.4037T>C
NM_001363725.2:c.1494T>C	NP_001350654.1:p.Gly498=
NM_001371656.1:c.3873T>C	NP_001358585.1:p.Gly1291=
NM_001374820.1:c.3873T>C	NP_001361749.1:p.Gly1291=
NM_001374828.1:c.3993T>C MANE Select	NP_001361757.1:p.Gly1331=
NM_017519.3:c.3834T>C	NP_059989.3:p.Gly1278=