Canonical Allele Identifier: CA452978388

Gene: ARID1B

Linked Data

• dbSNP Id: rs757252042
• gnomAD v4: 6-157201355-C-T
• MyVariant Identifiers: chr6:g.157522489C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201355C>T , CM000668.2:g.157201355C>T	GRCh38
NC_000006.11:g.157522489C>T , CM000668.1:g.157522489C>T	GRCh37
NC_000006.10:g.157564181C>T	NCBI36
NG_032093.1:g.428426C>T
NG_032093.2:g.428426C>T
NG_066624.1:g.430330C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4971C>T	ENSP00000055163.8:p.Val1657=
ENST00000414678.8:c.5040C>T	ENSP00000412835.3:p.Val1680=
ENST00000637015.2:c.5259C>T	ENSP00000489729.2:p.Val1753=
ENST00000346085.10:c.5010C>T	ENSP00000344546.5:p.Val1670=
ENST00000350026.10:c.4722C>T	ENSP00000055163.7:p.Val1574=
ENST00000414678.7:c.3288C>T	ENSP00000412835.2:p.Val1096=
ENST00000635849.1:c.2451C>T	ENSP00000490948.1:p.Val817=
ENST00000635957.1:c.2082C>T	ENSP00000490385.1:p.Val694=
ENST00000636227.1:n.3593C>T
ENST00000636254.1:n.1050C>T
ENST00000636930.2:c.5130C>T MANE Select	ENSP00000490491.2:p.Val1710=
ENST00000636940.1:n.3127C>T
ENST00000637015.1:c.2498C>T
ENST00000637568.1:c.2412C>T
ENST00000637741.1:n.1796C>T
ENST00000637810.1:c.2472C>T	ENSP00000489636.1:p.Val824=
ENST00000637904.1:c.2631C>T	ENSP00000490550.1:p.Val877=
ENST00000647938.1:c.4761C>T	ENSP00000498155.1:p.Val1587=
ENST00000346085.9:c.4761C>T	ENSP00000344546.4:p.Val1587=
ENST00000350026.9:c.4722C>T	ENSP00000055163.7:p.Val1574=
ENST00000414678.6:c.3288C>T	ENSP00000412835.2:p.Val1096=
NM_017519.2:c.4722C>T	NP_059989.2:p.Val1574=
NM_020732.3:c.4761C>T	NP_065783.3:p.Val1587=
XM_005267069.3:c.4881C>T	XP_005267126.2:p.Val1627=
XM_011535984.1:c.3960C>T	XP_011534286.1:p.Val1320=
XM_011535985.1:c.3780C>T	XP_011534287.1:p.Val1260=
XM_011535986.1:c.3540C>T	XP_011534288.1:p.Val1180=
XM_011535987.1:c.3159C>T	XP_011534289.1:p.Val1053=
XM_011535988.1:c.2022C>T	XP_011534290.1:p.Val674=
NM_001346813.1:c.4881C>T	NP_001333742.1:p.Val1627=
NM_001363725.1:c.2631C>T	NP_001350654.1:p.Val877=
XM_011535984.2:c.5091C>T	XP_011534286.2:p.Val1697=
XM_011535988.3:c.2022C>T	XP_011534290.1:p.Val674=
XM_017011103.2:c.4992C>T	XP_016866592.1:p.Val1664=
XM_017011104.1:c.4962C>T	XP_016866593.1:p.Val1654=
XM_017011105.2:c.4932C>T	XP_016866594.1:p.Val1644=
XM_017011106.2:c.4803C>T	XP_016866595.1:p.Val1601=
XM_017011107.2:c.4782C>T	XP_016866596.1:p.Val1594=
XR_002956289.1:n.5077C>T
NM_001363725.2:c.2631C>T	NP_001350654.1:p.Val877=
NM_001371656.1:c.5010C>T	NP_001358585.1:p.Val1670=
NM_001374820.1:c.5010C>T	NP_001361749.1:p.Val1670=
NM_001374828.1:c.5130C>T MANE Select	NP_001361757.1:p.Val1710=
NM_017519.3:c.4971C>T	NP_059989.3:p.Val1657=