Canonical Allele Identifier: CA366235188

Gene: ARID1B

Linked Data

• dbSNP Id: rs150196933
• MyVariant Identifiers: chr6:g.157511228C>A (hg19) ; chr6:g.157190094C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190094C>A , CM000668.2:g.157190094C>A	GRCh38
NC_000006.11:g.157511228C>A , CM000668.1:g.157511228C>A	GRCh37
NC_000006.10:g.157552920C>A	NCBI36
NG_032093.1:g.417165C>A
NG_032093.2:g.417165C>A
NG_066624.1:g.419069C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3956C>A	ENSP00000055163.8:p.Pro1319Gln
ENST00000414678.8:c.4025C>A	ENSP00000412835.3:p.Pro1342Gln
ENST00000637015.2:c.4244C>A	ENSP00000489729.2:p.Pro1415Gln
ENST00000346085.10:c.3995C>A	ENSP00000344546.5:p.Pro1332Gln
ENST00000350026.10:c.3707C>A	ENSP00000055163.7:p.Pro1236Gln
ENST00000414678.7:c.2273C>A	ENSP00000412835.2:p.Pro758Gln
ENST00000635849.1:c.1436C>A	ENSP00000490948.1:p.Pro479Gln
ENST00000635957.1:c.1067C>A	ENSP00000490385.1:p.Pro356Gln
ENST00000636930.2:c.4115C>A MANE Select	ENSP00000490491.2:p.Pro1372Gln
ENST00000636940.1:n.2112C>A
ENST00000637015.1:c.1483C>A
ENST00000637568.1:c.1397C>A
ENST00000637741.1:n.781C>A
ENST00000637810.1:c.1457C>A	ENSP00000489636.1:p.Pro486Gln
ENST00000637904.1:c.1616C>A	ENSP00000490550.1:p.Pro539Gln
ENST00000647938.1:c.3746C>A	ENSP00000498155.1:p.Pro1249Gln
ENST00000346085.9:c.3746C>A	ENSP00000344546.4:p.Pro1249Gln
ENST00000350026.9:c.3707C>A	ENSP00000055163.7:p.Pro1236Gln
ENST00000414678.6:c.2273C>A	ENSP00000412835.2:p.Pro758Gln
NM_017519.2:c.3707C>A	NP_059989.2:p.Pro1236Gln
NM_020732.3:c.3746C>A	NP_065783.3:p.Pro1249Gln
XM_005267069.3:c.3866C>A	XP_005267126.2:p.Pro1289Gln
XM_011535984.1:c.2945C>A	XP_011534286.1:p.Pro982Gln
XM_011535985.1:c.2765C>A	XP_011534287.1:p.Pro922Gln
XM_011535986.1:c.2525C>A	XP_011534288.1:p.Pro842Gln
XM_011535987.1:c.2144C>A	XP_011534289.1:p.Pro715Gln
XM_011535988.1:c.1007C>A	XP_011534290.1:p.Pro336Gln
NM_001346813.1:c.3866C>A	NP_001333742.1:p.Pro1289Gln
NM_001363725.1:c.1616C>A	NP_001350654.1:p.Pro539Gln
XM_011535984.2:c.4076C>A	XP_011534286.2:p.Pro1359Gln
XM_011535988.3:c.1007C>A	XP_011534290.1:p.Pro336Gln
XM_017011103.2:c.3977C>A	XP_016866592.1:p.Pro1326Gln
XM_017011104.1:c.3947C>A	XP_016866593.1:p.Pro1316Gln
XM_017011105.2:c.3917C>A	XP_016866594.1:p.Pro1306Gln
XM_017011106.2:c.3788C>A	XP_016866595.1:p.Pro1263Gln
XM_017011107.2:c.3767C>A	XP_016866596.1:p.Pro1256Gln
XR_002956289.1:n.4159C>A
NM_001363725.2:c.1616C>A	NP_001350654.1:p.Pro539Gln
NM_001371656.1:c.3995C>A	NP_001358585.1:p.Pro1332Gln
NM_001374820.1:c.3995C>A	NP_001361749.1:p.Pro1332Gln
NM_001374828.1:c.4115C>A MANE Select	NP_001361757.1:p.Pro1372Gln
NM_017519.3:c.3956C>A	NP_059989.3:p.Pro1319Gln