Canonical Allele Identifier: CA452781528

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510843T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189709T>A , CM000668.2:g.157189709T>A	GRCh38
NC_000006.11:g.157510843T>A , CM000668.1:g.157510843T>A	GRCh37
NC_000006.10:g.157552535T>A	NCBI36
NG_032093.1:g.416780T>A
NG_032093.2:g.416780T>A
NG_066624.1:g.418684T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3828T>A	ENSP00000055163.8:p.Val1276=
ENST00000414678.8:c.3897T>A	ENSP00000412835.3:p.Val1299=
ENST00000637015.2:c.4116T>A	ENSP00000489729.2:p.Val1372=
ENST00000346085.10:c.3867T>A	ENSP00000344546.5:p.Val1289=
ENST00000350026.10:c.3579T>A	ENSP00000055163.7:p.Val1193=
ENST00000414678.7:c.2145T>A	ENSP00000412835.2:p.Val715=
ENST00000635849.1:c.1308T>A	ENSP00000490948.1:p.Val436=
ENST00000635957.1:c.942T>A	ENSP00000490385.1:p.Val314=
ENST00000636930.2:c.3987T>A MANE Select	ENSP00000490491.2:p.Val1329=
ENST00000636940.1:n.1984T>A
ENST00000637015.1:c.1355T>A
ENST00000637568.1:c.1269T>A
ENST00000637741.1:n.653T>A
ENST00000637810.1:c.1329T>A	ENSP00000489636.1:p.Val443=
ENST00000637904.1:c.1488T>A	ENSP00000490550.1:p.Val496=
ENST00000647938.1:c.3618T>A	ENSP00000498155.1:p.Val1206=
ENST00000346085.9:c.3618T>A	ENSP00000344546.4:p.Val1206=
ENST00000350026.9:c.3579T>A	ENSP00000055163.7:p.Val1193=
ENST00000414678.6:c.2145T>A	ENSP00000412835.2:p.Val715=
NM_017519.2:c.3579T>A	NP_059989.2:p.Val1193=
NM_020732.3:c.3618T>A	NP_065783.3:p.Val1206=
XM_005267069.3:c.3738T>A	XP_005267126.2:p.Val1246=
XM_011535984.1:c.2817T>A	XP_011534286.1:p.Val939=
XM_011535985.1:c.2637T>A	XP_011534287.1:p.Val879=
XM_011535986.1:c.2397T>A	XP_011534288.1:p.Val799=
XM_011535987.1:c.2016T>A	XP_011534289.1:p.Val672=
XM_011535988.1:c.879T>A	XP_011534290.1:p.Val293=
NM_001346813.1:c.3738T>A	NP_001333742.1:p.Val1246=
NM_001363725.1:c.1488T>A	NP_001350654.1:p.Val496=
XM_011535984.2:c.3948T>A	XP_011534286.2:p.Val1316=
XM_011535988.3:c.879T>A	XP_011534290.1:p.Val293=
XM_017011103.2:c.3849T>A	XP_016866592.1:p.Val1283=
XM_017011104.1:c.3819T>A	XP_016866593.1:p.Val1273=
XM_017011105.2:c.3789T>A	XP_016866594.1:p.Val1263=
XM_017011106.2:c.3660T>A	XP_016866595.1:p.Val1220=
XM_017011107.2:c.3639T>A	XP_016866596.1:p.Val1213=
XR_002956289.1:n.4031T>A
NM_001363725.2:c.1488T>A	NP_001350654.1:p.Val496=
NM_001371656.1:c.3867T>A	NP_001358585.1:p.Val1289=
NM_001374820.1:c.3867T>A	NP_001361749.1:p.Val1289=
NM_001374828.1:c.3987T>A MANE Select	NP_001361757.1:p.Val1329=
NM_017519.3:c.3828T>A	NP_059989.3:p.Val1276=