Canonical Allele Identifier: CA452781551

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510870A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189736A>G , CM000668.2:g.157189736A>G	GRCh38
NC_000006.11:g.157510870A>G , CM000668.1:g.157510870A>G	GRCh37
NC_000006.10:g.157552562A>G	NCBI36
NG_032093.1:g.416807A>G
NG_032093.2:g.416807A>G
NG_066624.1:g.418711A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3855A>G	ENSP00000055163.8:p.Pro1285=
ENST00000414678.8:c.3924A>G	ENSP00000412835.3:p.Pro1308=
ENST00000637015.2:c.4143A>G	ENSP00000489729.2:p.Pro1381=
ENST00000346085.10:c.3894A>G	ENSP00000344546.5:p.Pro1298=
ENST00000350026.10:c.3606A>G	ENSP00000055163.7:p.Pro1202=
ENST00000414678.7:c.2172A>G	ENSP00000412835.2:p.Pro724=
ENST00000635849.1:c.1335A>G	ENSP00000490948.1:p.Pro445=
ENST00000635957.1:c.969A>G	ENSP00000490385.1:p.Pro323=
ENST00000636930.2:c.4014A>G MANE Select	ENSP00000490491.2:p.Pro1338=
ENST00000636940.1:n.2011A>G
ENST00000637015.1:c.1382A>G
ENST00000637568.1:c.1296A>G
ENST00000637741.1:n.680A>G
ENST00000637810.1:c.1356A>G	ENSP00000489636.1:p.Pro452=
ENST00000637904.1:c.1515A>G	ENSP00000490550.1:p.Pro505=
ENST00000647938.1:c.3645A>G	ENSP00000498155.1:p.Pro1215=
ENST00000346085.9:c.3645A>G	ENSP00000344546.4:p.Pro1215=
ENST00000350026.9:c.3606A>G	ENSP00000055163.7:p.Pro1202=
ENST00000414678.6:c.2172A>G	ENSP00000412835.2:p.Pro724=
NM_017519.2:c.3606A>G	NP_059989.2:p.Pro1202=
NM_020732.3:c.3645A>G	NP_065783.3:p.Pro1215=
XM_005267069.3:c.3765A>G	XP_005267126.2:p.Pro1255=
XM_011535984.1:c.2844A>G	XP_011534286.1:p.Pro948=
XM_011535985.1:c.2664A>G	XP_011534287.1:p.Pro888=
XM_011535986.1:c.2424A>G	XP_011534288.1:p.Pro808=
XM_011535987.1:c.2043A>G	XP_011534289.1:p.Pro681=
XM_011535988.1:c.906A>G	XP_011534290.1:p.Pro302=
NM_001346813.1:c.3765A>G	NP_001333742.1:p.Pro1255=
NM_001363725.1:c.1515A>G	NP_001350654.1:p.Pro505=
XM_011535984.2:c.3975A>G	XP_011534286.2:p.Pro1325=
XM_011535988.3:c.906A>G	XP_011534290.1:p.Pro302=
XM_017011103.2:c.3876A>G	XP_016866592.1:p.Pro1292=
XM_017011104.1:c.3846A>G	XP_016866593.1:p.Pro1282=
XM_017011105.2:c.3816A>G	XP_016866594.1:p.Pro1272=
XM_017011106.2:c.3687A>G	XP_016866595.1:p.Pro1229=
XM_017011107.2:c.3666A>G	XP_016866596.1:p.Pro1222=
XR_002956289.1:n.4058A>G
NM_001363725.2:c.1515A>G	NP_001350654.1:p.Pro505=
NM_001371656.1:c.3894A>G	NP_001358585.1:p.Pro1298=
NM_001374820.1:c.3894A>G	NP_001361749.1:p.Pro1298=
NM_001374828.1:c.4014A>G MANE Select	NP_001361757.1:p.Pro1338=
NM_017519.3:c.3855A>G	NP_059989.3:p.Pro1285=