Canonical Allele Identifier: CA366235322

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511258C>G (hg19) ; chr6:g.157190124C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190124C>G , CM000668.2:g.157190124C>G	GRCh38
NC_000006.11:g.157511258C>G , CM000668.1:g.157511258C>G	GRCh37
NC_000006.10:g.157552950C>G	NCBI36
NG_032093.1:g.417195C>G
NG_032093.2:g.417195C>G
NG_066624.1:g.419099C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3986C>G	ENSP00000055163.8:p.Pro1329Arg
ENST00000414678.8:c.4055C>G	ENSP00000412835.3:p.Pro1352Arg
ENST00000637015.2:c.4274C>G	ENSP00000489729.2:p.Pro1425Arg
ENST00000346085.10:c.4025C>G	ENSP00000344546.5:p.Pro1342Arg
ENST00000350026.10:c.3737C>G	ENSP00000055163.7:p.Pro1246Arg
ENST00000414678.7:c.2303C>G	ENSP00000412835.2:p.Pro768Arg
ENST00000635849.1:c.1466C>G	ENSP00000490948.1:p.Pro489Arg
ENST00000635957.1:c.1097C>G	ENSP00000490385.1:p.Pro366Arg
ENST00000636930.2:c.4145C>G MANE Select	ENSP00000490491.2:p.Pro1382Arg
ENST00000636940.1:n.2142C>G
ENST00000637015.1:c.1513C>G
ENST00000637568.1:c.1427C>G
ENST00000637741.1:n.811C>G
ENST00000637810.1:c.1487C>G	ENSP00000489636.1:p.Pro496Arg
ENST00000637904.1:c.1646C>G	ENSP00000490550.1:p.Pro549Arg
ENST00000647938.1:c.3776C>G	ENSP00000498155.1:p.Pro1259Arg
ENST00000346085.9:c.3776C>G	ENSP00000344546.4:p.Pro1259Arg
ENST00000350026.9:c.3737C>G	ENSP00000055163.7:p.Pro1246Arg
ENST00000414678.6:c.2303C>G	ENSP00000412835.2:p.Pro768Arg
NM_017519.2:c.3737C>G	NP_059989.2:p.Pro1246Arg
NM_020732.3:c.3776C>G	NP_065783.3:p.Pro1259Arg
XM_005267069.3:c.3896C>G	XP_005267126.2:p.Pro1299Arg
XM_011535984.1:c.2975C>G	XP_011534286.1:p.Pro992Arg
XM_011535985.1:c.2795C>G	XP_011534287.1:p.Pro932Arg
XM_011535986.1:c.2555C>G	XP_011534288.1:p.Pro852Arg
XM_011535987.1:c.2174C>G	XP_011534289.1:p.Pro725Arg
XM_011535988.1:c.1037C>G	XP_011534290.1:p.Pro346Arg
NM_001346813.1:c.3896C>G	NP_001333742.1:p.Pro1299Arg
NM_001363725.1:c.1646C>G	NP_001350654.1:p.Pro549Arg
XM_011535984.2:c.4106C>G	XP_011534286.2:p.Pro1369Arg
XM_011535988.3:c.1037C>G	XP_011534290.1:p.Pro346Arg
XM_017011103.2:c.4007C>G	XP_016866592.1:p.Pro1336Arg
XM_017011104.1:c.3977C>G	XP_016866593.1:p.Pro1326Arg
XM_017011105.2:c.3947C>G	XP_016866594.1:p.Pro1316Arg
XM_017011106.2:c.3818C>G	XP_016866595.1:p.Pro1273Arg
XM_017011107.2:c.3797C>G	XP_016866596.1:p.Pro1266Arg
XR_002956289.1:n.4189C>G
NM_001363725.2:c.1646C>G	NP_001350654.1:p.Pro549Arg
NM_001371656.1:c.4025C>G	NP_001358585.1:p.Pro1342Arg
NM_001374820.1:c.4025C>G	NP_001361749.1:p.Pro1342Arg
NM_001374828.1:c.4145C>G MANE Select	NP_001361757.1:p.Pro1382Arg
NM_017519.3:c.3986C>G	NP_059989.3:p.Pro1329Arg