Canonical Allele Identifier: CA452781577

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510912A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189778A>C , CM000668.2:g.157189778A>C	GRCh38
NC_000006.11:g.157510912A>C , CM000668.1:g.157510912A>C	GRCh37
NC_000006.10:g.157552604A>C	NCBI36
NG_032093.1:g.416849A>C
NG_032093.2:g.416849A>C
NG_066624.1:g.418753A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3897A>C	ENSP00000055163.8:p.Gly1299=
ENST00000414678.8:c.3966A>C	ENSP00000412835.3:p.Gly1322=
ENST00000637015.2:c.4185A>C	ENSP00000489729.2:p.Gly1395=
ENST00000346085.10:c.3936A>C	ENSP00000344546.5:p.Gly1312=
ENST00000350026.10:c.3648A>C	ENSP00000055163.7:p.Gly1216=
ENST00000414678.7:c.2214A>C	ENSP00000412835.2:p.Gly738=
ENST00000635849.1:c.1377A>C	ENSP00000490948.1:p.Gly459=
ENST00000635957.1:c.1011A>C	ENSP00000490385.1:p.Gly337=
ENST00000636930.2:c.4056A>C MANE Select	ENSP00000490491.2:p.Gly1352=
ENST00000636940.1:n.2053A>C
ENST00000637015.1:c.1424A>C
ENST00000637568.1:c.1338A>C
ENST00000637741.1:n.722A>C
ENST00000637810.1:c.1398A>C	ENSP00000489636.1:p.Gly466=
ENST00000637904.1:c.1557A>C	ENSP00000490550.1:p.Gly519=
ENST00000647938.1:c.3687A>C	ENSP00000498155.1:p.Gly1229=
ENST00000346085.9:c.3687A>C	ENSP00000344546.4:p.Gly1229=
ENST00000350026.9:c.3648A>C	ENSP00000055163.7:p.Gly1216=
ENST00000414678.6:c.2214A>C	ENSP00000412835.2:p.Gly738=
NM_017519.2:c.3648A>C	NP_059989.2:p.Gly1216=
NM_020732.3:c.3687A>C	NP_065783.3:p.Gly1229=
XM_005267069.3:c.3807A>C	XP_005267126.2:p.Gly1269=
XM_011535984.1:c.2886A>C	XP_011534286.1:p.Gly962=
XM_011535985.1:c.2706A>C	XP_011534287.1:p.Gly902=
XM_011535986.1:c.2466A>C	XP_011534288.1:p.Gly822=
XM_011535987.1:c.2085A>C	XP_011534289.1:p.Gly695=
XM_011535988.1:c.948A>C	XP_011534290.1:p.Gly316=
NM_001346813.1:c.3807A>C	NP_001333742.1:p.Gly1269=
NM_001363725.1:c.1557A>C	NP_001350654.1:p.Gly519=
XM_011535984.2:c.4017A>C	XP_011534286.2:p.Gly1339=
XM_011535988.3:c.948A>C	XP_011534290.1:p.Gly316=
XM_017011103.2:c.3918A>C	XP_016866592.1:p.Gly1306=
XM_017011104.1:c.3888A>C	XP_016866593.1:p.Gly1296=
XM_017011105.2:c.3858A>C	XP_016866594.1:p.Gly1286=
XM_017011106.2:c.3729A>C	XP_016866595.1:p.Gly1243=
XM_017011107.2:c.3708A>C	XP_016866596.1:p.Gly1236=
XR_002956289.1:n.4100A>C
NM_001363725.2:c.1557A>C	NP_001350654.1:p.Gly519=
NM_001371656.1:c.3936A>C	NP_001358585.1:p.Gly1312=
NM_001374820.1:c.3936A>C	NP_001361749.1:p.Gly1312=
NM_001374828.1:c.4056A>C MANE Select	NP_001361757.1:p.Gly1352=
NM_017519.3:c.3897A>C	NP_059989.3:p.Gly1299=