Canonical Allele Identifier: CA366235254

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511233C>G (hg19) ; chr6:g.157190099C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3961C>G	ENSP00000055163.8:p.Arg1321Gly
ENST00000414678.8:c.4030C>G	ENSP00000412835.3:p.Arg1344Gly
ENST00000637015.2:c.4249C>G	ENSP00000489729.2:p.Arg1417Gly
ENST00000346085.10:c.4000C>G	ENSP00000344546.5:p.Arg1334Gly
ENST00000350026.10:c.3712C>G	ENSP00000055163.7:p.Arg1238Gly
ENST00000414678.7:c.2278C>G	ENSP00000412835.2:p.Arg760Gly
ENST00000635849.1:c.1441C>G	ENSP00000490948.1:p.Arg481Gly
ENST00000635957.1:c.1072C>G	ENSP00000490385.1:p.Arg358Gly
ENST00000636930.2:c.4120C>G MANE Select	ENSP00000490491.2:p.Arg1374Gly
ENST00000636940.1:n.2117C>G
ENST00000637015.1:c.1488C>G
ENST00000637568.1:c.1402C>G
ENST00000637741.1:n.786C>G
ENST00000637810.1:c.1462C>G	ENSP00000489636.1:p.Arg488Gly
ENST00000637904.1:c.1621C>G	ENSP00000490550.1:p.Arg541Gly
ENST00000647938.1:c.3751C>G	ENSP00000498155.1:p.Arg1251Gly
ENST00000346085.9:c.3751C>G	ENSP00000344546.4:p.Arg1251Gly
ENST00000350026.9:c.3712C>G	ENSP00000055163.7:p.Arg1238Gly
ENST00000414678.6:c.2278C>G	ENSP00000412835.2:p.Arg760Gly
NM_017519.2:c.3712C>G	NP_059989.2:p.Arg1238Gly
NM_020732.3:c.3751C>G	NP_065783.3:p.Arg1251Gly
XM_005267069.3:c.3871C>G	XP_005267126.2:p.Arg1291Gly
XM_011535984.1:c.2950C>G	XP_011534286.1:p.Arg984Gly
XM_011535985.1:c.2770C>G	XP_011534287.1:p.Arg924Gly
XM_011535986.1:c.2530C>G	XP_011534288.1:p.Arg844Gly
XM_011535987.1:c.2149C>G	XP_011534289.1:p.Arg717Gly
XM_011535988.1:c.1012C>G	XP_011534290.1:p.Arg338Gly
NM_001346813.1:c.3871C>G	NP_001333742.1:p.Arg1291Gly
NM_001363725.1:c.1621C>G	NP_001350654.1:p.Arg541Gly
XM_011535984.2:c.4081C>G	XP_011534286.2:p.Arg1361Gly
XM_011535988.3:c.1012C>G	XP_011534290.1:p.Arg338Gly
XM_017011103.2:c.3982C>G	XP_016866592.1:p.Arg1328Gly
XM_017011104.1:c.3952C>G	XP_016866593.1:p.Arg1318Gly
XM_017011105.2:c.3922C>G	XP_016866594.1:p.Arg1308Gly
XM_017011106.2:c.3793C>G	XP_016866595.1:p.Arg1265Gly
XM_017011107.2:c.3772C>G	XP_016866596.1:p.Arg1258Gly
XR_002956289.1:n.4164C>G
NM_001363725.2:c.1621C>G	NP_001350654.1:p.Arg541Gly
NM_001371656.1:c.4000C>G	NP_001358585.1:p.Arg1334Gly
NM_001374820.1:c.4000C>G	NP_001361749.1:p.Arg1334Gly
NM_001374828.1:c.4120C>G MANE Select	NP_001361757.1:p.Arg1374Gly
NM_017519.3:c.3961C>G	NP_059989.3:p.Arg1321Gly