Canonical Allele Identifier: CA4067526

Gene: ARID1B

Linked Data

• dbSNP Id: rs754100748
• ExAC: 6:157511233 C / T
• gnomAD v2: 6-157511233-C-T
• gnomAD v3: 6-157190099-C-T
• gnomAD v4: 6-157190099-C-T
• MyVariant Identifiers: chr6:g.157511233C>T (hg19) ; chr6:g.157190099C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3961C>T	ENSP00000055163.8:p.Arg1321Trp
ENST00000414678.8:c.4030C>T	ENSP00000412835.3:p.Arg1344Trp
ENST00000637015.2:c.4249C>T	ENSP00000489729.2:p.Arg1417Trp
ENST00000346085.10:c.4000C>T	ENSP00000344546.5:p.Arg1334Trp
ENST00000350026.10:c.3712C>T	ENSP00000055163.7:p.Arg1238Trp
ENST00000414678.7:c.2278C>T	ENSP00000412835.2:p.Arg760Trp
ENST00000635849.1:c.1441C>T	ENSP00000490948.1:p.Arg481Trp
ENST00000635957.1:c.1072C>T	ENSP00000490385.1:p.Arg358Trp
ENST00000636930.2:c.4120C>T MANE Select	ENSP00000490491.2:p.Arg1374Trp
ENST00000636940.1:n.2117C>T
ENST00000637015.1:c.1488C>T
ENST00000637568.1:c.1402C>T
ENST00000637741.1:n.786C>T
ENST00000637810.1:c.1462C>T	ENSP00000489636.1:p.Arg488Trp
ENST00000637904.1:c.1621C>T	ENSP00000490550.1:p.Arg541Trp
ENST00000647938.1:c.3751C>T	ENSP00000498155.1:p.Arg1251Trp
ENST00000346085.9:c.3751C>T	ENSP00000344546.4:p.Arg1251Trp
ENST00000350026.9:c.3712C>T	ENSP00000055163.7:p.Arg1238Trp
ENST00000414678.6:c.2278C>T	ENSP00000412835.2:p.Arg760Trp
NM_017519.2:c.3712C>T	NP_059989.2:p.Arg1238Trp
NM_020732.3:c.3751C>T	NP_065783.3:p.Arg1251Trp
XM_005267069.3:c.3871C>T	XP_005267126.2:p.Arg1291Trp
XM_011535984.1:c.2950C>T	XP_011534286.1:p.Arg984Trp
XM_011535985.1:c.2770C>T	XP_011534287.1:p.Arg924Trp
XM_011535986.1:c.2530C>T	XP_011534288.1:p.Arg844Trp
XM_011535987.1:c.2149C>T	XP_011534289.1:p.Arg717Trp
XM_011535988.1:c.1012C>T	XP_011534290.1:p.Arg338Trp
NM_001346813.1:c.3871C>T	NP_001333742.1:p.Arg1291Trp
NM_001363725.1:c.1621C>T	NP_001350654.1:p.Arg541Trp
XM_011535984.2:c.4081C>T	XP_011534286.2:p.Arg1361Trp
XM_011535988.3:c.1012C>T	XP_011534290.1:p.Arg338Trp
XM_017011103.2:c.3982C>T	XP_016866592.1:p.Arg1328Trp
XM_017011104.1:c.3952C>T	XP_016866593.1:p.Arg1318Trp
XM_017011105.2:c.3922C>T	XP_016866594.1:p.Arg1308Trp
XM_017011106.2:c.3793C>T	XP_016866595.1:p.Arg1265Trp
XM_017011107.2:c.3772C>T	XP_016866596.1:p.Arg1258Trp
XR_002956289.1:n.4164C>T
NM_001363725.2:c.1621C>T	NP_001350654.1:p.Arg541Trp
NM_001371656.1:c.4000C>T	NP_001358585.1:p.Arg1334Trp
NM_001374820.1:c.4000C>T	NP_001361749.1:p.Arg1334Trp
NM_001374828.1:c.4120C>T MANE Select	NP_001361757.1:p.Arg1374Trp
NM_017519.3:c.3961C>T	NP_059989.3:p.Arg1321Trp