Canonical Allele Identifier: CA366234193

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128338982
• MyVariant Identifiers: chr6:g.157510872C>T (hg19) ; chr6:g.157189738C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189738C>T , CM000668.2:g.157189738C>T	GRCh38
NC_000006.11:g.157510872C>T , CM000668.1:g.157510872C>T	GRCh37
NC_000006.10:g.157552564C>T	NCBI36
NG_032093.1:g.416809C>T
NG_032093.2:g.416809C>T
NG_066624.1:g.418713C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3857C>T	ENSP00000055163.8:p.Ala1286Val
ENST00000414678.8:c.3926C>T	ENSP00000412835.3:p.Ala1309Val
ENST00000637015.2:c.4145C>T	ENSP00000489729.2:p.Ala1382Val
ENST00000346085.10:c.3896C>T	ENSP00000344546.5:p.Ala1299Val
ENST00000350026.10:c.3608C>T	ENSP00000055163.7:p.Ala1203Val
ENST00000414678.7:c.2174C>T	ENSP00000412835.2:p.Ala725Val
ENST00000635849.1:c.1337C>T	ENSP00000490948.1:p.Ala446Val
ENST00000635957.1:c.971C>T	ENSP00000490385.1:p.Ala324Val
ENST00000636930.2:c.4016C>T MANE Select	ENSP00000490491.2:p.Ala1339Val
ENST00000636940.1:n.2013C>T
ENST00000637015.1:c.1384C>T
ENST00000637568.1:c.1298C>T
ENST00000637741.1:n.682C>T
ENST00000637810.1:c.1358C>T	ENSP00000489636.1:p.Ala453Val
ENST00000637904.1:c.1517C>T	ENSP00000490550.1:p.Ala506Val
ENST00000647938.1:c.3647C>T	ENSP00000498155.1:p.Ala1216Val
ENST00000346085.9:c.3647C>T	ENSP00000344546.4:p.Ala1216Val
ENST00000350026.9:c.3608C>T	ENSP00000055163.7:p.Ala1203Val
ENST00000414678.6:c.2174C>T	ENSP00000412835.2:p.Ala725Val
NM_017519.2:c.3608C>T	NP_059989.2:p.Ala1203Val
NM_020732.3:c.3647C>T	NP_065783.3:p.Ala1216Val
XM_005267069.3:c.3767C>T	XP_005267126.2:p.Ala1256Val
XM_011535984.1:c.2846C>T	XP_011534286.1:p.Ala949Val
XM_011535985.1:c.2666C>T	XP_011534287.1:p.Ala889Val
XM_011535986.1:c.2426C>T	XP_011534288.1:p.Ala809Val
XM_011535987.1:c.2045C>T	XP_011534289.1:p.Ala682Val
XM_011535988.1:c.908C>T	XP_011534290.1:p.Ala303Val
NM_001346813.1:c.3767C>T	NP_001333742.1:p.Ala1256Val
NM_001363725.1:c.1517C>T	NP_001350654.1:p.Ala506Val
XM_011535984.2:c.3977C>T	XP_011534286.2:p.Ala1326Val
XM_011535988.3:c.908C>T	XP_011534290.1:p.Ala303Val
XM_017011103.2:c.3878C>T	XP_016866592.1:p.Ala1293Val
XM_017011104.1:c.3848C>T	XP_016866593.1:p.Ala1283Val
XM_017011105.2:c.3818C>T	XP_016866594.1:p.Ala1273Val
XM_017011106.2:c.3689C>T	XP_016866595.1:p.Ala1230Val
XM_017011107.2:c.3668C>T	XP_016866596.1:p.Ala1223Val
XR_002956289.1:n.4060C>T
NM_001363725.2:c.1517C>T	NP_001350654.1:p.Ala506Val
NM_001371656.1:c.3896C>T	NP_001358585.1:p.Ala1299Val
NM_001374820.1:c.3896C>T	NP_001361749.1:p.Ala1299Val
NM_001374828.1:c.4016C>T MANE Select	NP_001361757.1:p.Ala1339Val
NM_017519.3:c.3857C>T	NP_059989.3:p.Ala1286Val