Canonical Allele Identifier: CA452781602

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511211G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190077G>T , CM000668.2:g.157190077G>T	GRCh38
NC_000006.11:g.157511211G>T , CM000668.1:g.157511211G>T	GRCh37
NC_000006.10:g.157552903G>T	NCBI36
NG_032093.1:g.417148G>T
NG_032093.2:g.417148G>T
NG_066624.1:g.419052G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3939G>T	ENSP00000055163.8:p.Val1313=
ENST00000414678.8:c.4008G>T	ENSP00000412835.3:p.Val1336=
ENST00000637015.2:c.4227G>T	ENSP00000489729.2:p.Val1409=
ENST00000346085.10:c.3978G>T	ENSP00000344546.5:p.Val1326=
ENST00000350026.10:c.3690G>T	ENSP00000055163.7:p.Val1230=
ENST00000414678.7:c.2256G>T	ENSP00000412835.2:p.Val752=
ENST00000635849.1:c.1419G>T	ENSP00000490948.1:p.Val473=
ENST00000635957.1:c.1050G>T	ENSP00000490385.1:p.Val350=
ENST00000636930.2:c.4098G>T MANE Select	ENSP00000490491.2:p.Val1366=
ENST00000636940.1:n.2095G>T
ENST00000637015.1:c.1466G>T
ENST00000637568.1:c.1380G>T
ENST00000637741.1:n.764G>T
ENST00000637810.1:c.1440G>T	ENSP00000489636.1:p.Val480=
ENST00000637904.1:c.1599G>T	ENSP00000490550.1:p.Val533=
ENST00000647938.1:c.3729G>T	ENSP00000498155.1:p.Val1243=
ENST00000346085.9:c.3729G>T	ENSP00000344546.4:p.Val1243=
ENST00000350026.9:c.3690G>T	ENSP00000055163.7:p.Val1230=
ENST00000414678.6:c.2256G>T	ENSP00000412835.2:p.Val752=
NM_017519.2:c.3690G>T	NP_059989.2:p.Val1230=
NM_020732.3:c.3729G>T	NP_065783.3:p.Val1243=
XM_005267069.3:c.3849G>T	XP_005267126.2:p.Val1283=
XM_011535984.1:c.2928G>T	XP_011534286.1:p.Val976=
XM_011535985.1:c.2748G>T	XP_011534287.1:p.Val916=
XM_011535986.1:c.2508G>T	XP_011534288.1:p.Val836=
XM_011535987.1:c.2127G>T	XP_011534289.1:p.Val709=
XM_011535988.1:c.990G>T	XP_011534290.1:p.Val330=
NM_001346813.1:c.3849G>T	NP_001333742.1:p.Val1283=
NM_001363725.1:c.1599G>T	NP_001350654.1:p.Val533=
XM_011535984.2:c.4059G>T	XP_011534286.2:p.Val1353=
XM_011535988.3:c.990G>T	XP_011534290.1:p.Val330=
XM_017011103.2:c.3960G>T	XP_016866592.1:p.Val1320=
XM_017011104.1:c.3930G>T	XP_016866593.1:p.Val1310=
XM_017011105.2:c.3900G>T	XP_016866594.1:p.Val1300=
XM_017011106.2:c.3771G>T	XP_016866595.1:p.Val1257=
XM_017011107.2:c.3750G>T	XP_016866596.1:p.Val1250=
XR_002956289.1:n.4142G>T
NM_001363725.2:c.1599G>T	NP_001350654.1:p.Val533=
NM_001371656.1:c.3978G>T	NP_001358585.1:p.Val1326=
NM_001374820.1:c.3978G>T	NP_001361749.1:p.Val1326=
NM_001374828.1:c.4098G>T MANE Select	NP_001361757.1:p.Val1366=
NM_017519.3:c.3939G>T	NP_059989.3:p.Val1313=