Canonical Allele Identifier: CA366234906

Gene: ARID1B

Linked Data

• dbSNP Id: rs1793246902
• MyVariant Identifiers: chr6:g.157511200T>G (hg19) ; chr6:g.157190066T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190066T>G , CM000668.2:g.157190066T>G	GRCh38
NC_000006.11:g.157511200T>G , CM000668.1:g.157511200T>G	GRCh37
NC_000006.10:g.157552892T>G	NCBI36
NG_032093.1:g.417137T>G
NG_032093.2:g.417137T>G
NG_066624.1:g.419041T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3928T>G	ENSP00000055163.8:p.Phe1310Val
ENST00000414678.8:c.3997T>G	ENSP00000412835.3:p.Phe1333Val
ENST00000637015.2:c.4216T>G	ENSP00000489729.2:p.Phe1406Val
ENST00000346085.10:c.3967T>G	ENSP00000344546.5:p.Phe1323Val
ENST00000350026.10:c.3679T>G	ENSP00000055163.7:p.Phe1227Val
ENST00000414678.7:c.2245T>G	ENSP00000412835.2:p.Phe749Val
ENST00000635849.1:c.1408T>G	ENSP00000490948.1:p.Phe470Val
ENST00000635957.1:c.1039T>G	ENSP00000490385.1:p.Phe347Val
ENST00000636930.2:c.4087T>G MANE Select	ENSP00000490491.2:p.Phe1363Val
ENST00000636940.1:n.2084T>G
ENST00000637015.1:c.1455T>G
ENST00000637568.1:c.1369T>G
ENST00000637741.1:n.753T>G
ENST00000637810.1:c.1429T>G	ENSP00000489636.1:p.Phe477Val
ENST00000637904.1:c.1588T>G	ENSP00000490550.1:p.Phe530Val
ENST00000647938.1:c.3718T>G	ENSP00000498155.1:p.Phe1240Val
ENST00000346085.9:c.3718T>G	ENSP00000344546.4:p.Phe1240Val
ENST00000350026.9:c.3679T>G	ENSP00000055163.7:p.Phe1227Val
ENST00000414678.6:c.2245T>G	ENSP00000412835.2:p.Phe749Val
NM_017519.2:c.3679T>G	NP_059989.2:p.Phe1227Val
NM_020732.3:c.3718T>G	NP_065783.3:p.Phe1240Val
XM_005267069.3:c.3838T>G	XP_005267126.2:p.Phe1280Val
XM_011535984.1:c.2917T>G	XP_011534286.1:p.Phe973Val
XM_011535985.1:c.2737T>G	XP_011534287.1:p.Phe913Val
XM_011535986.1:c.2497T>G	XP_011534288.1:p.Phe833Val
XM_011535987.1:c.2116T>G	XP_011534289.1:p.Phe706Val
XM_011535988.1:c.979T>G	XP_011534290.1:p.Phe327Val
NM_001346813.1:c.3838T>G	NP_001333742.1:p.Phe1280Val
NM_001363725.1:c.1588T>G	NP_001350654.1:p.Phe530Val
XM_011535984.2:c.4048T>G	XP_011534286.2:p.Phe1350Val
XM_011535988.3:c.979T>G	XP_011534290.1:p.Phe327Val
XM_017011103.2:c.3949T>G	XP_016866592.1:p.Phe1317Val
XM_017011104.1:c.3919T>G	XP_016866593.1:p.Phe1307Val
XM_017011105.2:c.3889T>G	XP_016866594.1:p.Phe1297Val
XM_017011106.2:c.3760T>G	XP_016866595.1:p.Phe1254Val
XM_017011107.2:c.3739T>G	XP_016866596.1:p.Phe1247Val
XR_002956289.1:n.4131T>G
NM_001363725.2:c.1588T>G	NP_001350654.1:p.Phe530Val
NM_001371656.1:c.3967T>G	NP_001358585.1:p.Phe1323Val
NM_001374820.1:c.3967T>G	NP_001361749.1:p.Phe1323Val
NM_001374828.1:c.4087T>G MANE Select	NP_001361757.1:p.Phe1363Val
NM_017519.3:c.3928T>G	NP_059989.3:p.Phe1310Val