Canonical Allele Identifier: CA452781846

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511233C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190099C>A , CM000668.2:g.157190099C>A	GRCh38
NC_000006.11:g.157511233C>A , CM000668.1:g.157511233C>A	GRCh37
NC_000006.10:g.157552925C>A	NCBI36
NG_032093.1:g.417170C>A
NG_032093.2:g.417170C>A
NG_066624.1:g.419074C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3961C>A	ENSP00000055163.8:p.Arg1321=
ENST00000414678.8:c.4030C>A	ENSP00000412835.3:p.Arg1344=
ENST00000637015.2:c.4249C>A	ENSP00000489729.2:p.Arg1417=
ENST00000346085.10:c.4000C>A	ENSP00000344546.5:p.Arg1334=
ENST00000350026.10:c.3712C>A	ENSP00000055163.7:p.Arg1238=
ENST00000414678.7:c.2278C>A	ENSP00000412835.2:p.Arg760=
ENST00000635849.1:c.1441C>A	ENSP00000490948.1:p.Arg481=
ENST00000635957.1:c.1072C>A	ENSP00000490385.1:p.Arg358=
ENST00000636930.2:c.4120C>A MANE Select	ENSP00000490491.2:p.Arg1374=
ENST00000636940.1:n.2117C>A
ENST00000637015.1:c.1488C>A
ENST00000637568.1:c.1402C>A
ENST00000637741.1:n.786C>A
ENST00000637810.1:c.1462C>A	ENSP00000489636.1:p.Arg488=
ENST00000637904.1:c.1621C>A	ENSP00000490550.1:p.Arg541=
ENST00000647938.1:c.3751C>A	ENSP00000498155.1:p.Arg1251=
ENST00000346085.9:c.3751C>A	ENSP00000344546.4:p.Arg1251=
ENST00000350026.9:c.3712C>A	ENSP00000055163.7:p.Arg1238=
ENST00000414678.6:c.2278C>A	ENSP00000412835.2:p.Arg760=
NM_017519.2:c.3712C>A	NP_059989.2:p.Arg1238=
NM_020732.3:c.3751C>A	NP_065783.3:p.Arg1251=
XM_005267069.3:c.3871C>A	XP_005267126.2:p.Arg1291=
XM_011535984.1:c.2950C>A	XP_011534286.1:p.Arg984=
XM_011535985.1:c.2770C>A	XP_011534287.1:p.Arg924=
XM_011535986.1:c.2530C>A	XP_011534288.1:p.Arg844=
XM_011535987.1:c.2149C>A	XP_011534289.1:p.Arg717=
XM_011535988.1:c.1012C>A	XP_011534290.1:p.Arg338=
NM_001346813.1:c.3871C>A	NP_001333742.1:p.Arg1291=
NM_001363725.1:c.1621C>A	NP_001350654.1:p.Arg541=
XM_011535984.2:c.4081C>A	XP_011534286.2:p.Arg1361=
XM_011535988.3:c.1012C>A	XP_011534290.1:p.Arg338=
XM_017011103.2:c.3982C>A	XP_016866592.1:p.Arg1328=
XM_017011104.1:c.3952C>A	XP_016866593.1:p.Arg1318=
XM_017011105.2:c.3922C>A	XP_016866594.1:p.Arg1308=
XM_017011106.2:c.3793C>A	XP_016866595.1:p.Arg1265=
XM_017011107.2:c.3772C>A	XP_016866596.1:p.Arg1258=
XR_002956289.1:n.4164C>A
NM_001363725.2:c.1621C>A	NP_001350654.1:p.Arg541=
NM_001371656.1:c.4000C>A	NP_001358585.1:p.Arg1334=
NM_001374820.1:c.4000C>A	NP_001361749.1:p.Arg1334=
NM_001374828.1:c.4120C>A MANE Select	NP_001361757.1:p.Arg1374=
NM_017519.3:c.3961C>A	NP_059989.3:p.Arg1321=