Canonical Allele Identifier: CA452784778

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376322
• MyVariant Identifiers: chr6:g.157522504C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201370C>G , CM000668.2:g.157201370C>G	GRCh38
NC_000006.11:g.157522504C>G , CM000668.1:g.157522504C>G	GRCh37
NC_000006.10:g.157564196C>G	NCBI36
NG_032093.1:g.428441C>G
NG_032093.2:g.428441C>G
NG_066624.1:g.430345C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4986C>G	ENSP00000055163.8:p.Val1662=
ENST00000414678.8:c.5055C>G	ENSP00000412835.3:p.Val1685=
ENST00000637015.2:c.5274C>G	ENSP00000489729.2:p.Val1758=
ENST00000346085.10:c.5025C>G	ENSP00000344546.5:p.Val1675=
ENST00000350026.10:c.4737C>G	ENSP00000055163.7:p.Val1579=
ENST00000414678.7:c.3303C>G	ENSP00000412835.2:p.Val1101=
ENST00000635849.1:c.2466C>G	ENSP00000490948.1:p.Val822=
ENST00000635957.1:c.2097C>G	ENSP00000490385.1:p.Val699=
ENST00000636227.1:n.3608C>G
ENST00000636254.1:n.1065C>G
ENST00000636930.2:c.5145C>G MANE Select	ENSP00000490491.2:p.Val1715=
ENST00000636940.1:n.3142C>G
ENST00000637015.1:c.2513C>G
ENST00000637568.1:c.2427C>G
ENST00000637741.1:n.1811C>G
ENST00000637810.1:c.2487C>G	ENSP00000489636.1:p.Val829=
ENST00000637904.1:c.2646C>G	ENSP00000490550.1:p.Val882=
ENST00000647938.1:c.4776C>G	ENSP00000498155.1:p.Val1592=
ENST00000346085.9:c.4776C>G	ENSP00000344546.4:p.Val1592=
ENST00000350026.9:c.4737C>G	ENSP00000055163.7:p.Val1579=
ENST00000414678.6:c.3303C>G	ENSP00000412835.2:p.Val1101=
NM_017519.2:c.4737C>G	NP_059989.2:p.Val1579=
NM_020732.3:c.4776C>G	NP_065783.3:p.Val1592=
XM_005267069.3:c.4896C>G	XP_005267126.2:p.Val1632=
XM_011535984.1:c.3975C>G	XP_011534286.1:p.Val1325=
XM_011535985.1:c.3795C>G	XP_011534287.1:p.Val1265=
XM_011535986.1:c.3555C>G	XP_011534288.1:p.Val1185=
XM_011535987.1:c.3174C>G	XP_011534289.1:p.Val1058=
XM_011535988.1:c.2037C>G	XP_011534290.1:p.Val679=
NM_001346813.1:c.4896C>G	NP_001333742.1:p.Val1632=
NM_001363725.1:c.2646C>G	NP_001350654.1:p.Val882=
XM_011535984.2:c.5106C>G	XP_011534286.2:p.Val1702=
XM_011535988.3:c.2037C>G	XP_011534290.1:p.Val679=
XM_017011103.2:c.5007C>G	XP_016866592.1:p.Val1669=
XM_017011104.1:c.4977C>G	XP_016866593.1:p.Val1659=
XM_017011105.2:c.4947C>G	XP_016866594.1:p.Val1649=
XM_017011106.2:c.4818C>G	XP_016866595.1:p.Val1606=
XM_017011107.2:c.4797C>G	XP_016866596.1:p.Val1599=
XR_002956289.1:n.5092C>G
NM_001363725.2:c.2646C>G	NP_001350654.1:p.Val882=
NM_001371656.1:c.5025C>G	NP_001358585.1:p.Val1675=
NM_001374820.1:c.5025C>G	NP_001361749.1:p.Val1675=
NM_001374828.1:c.5145C>G MANE Select	NP_001361757.1:p.Val1715=
NM_017519.3:c.4986C>G	NP_059989.3:p.Val1662=