Canonical Allele Identifier: CA452784820

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201391-A-T
• MyVariant Identifiers: chr6:g.157522525A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201391A>T , CM000668.2:g.157201391A>T	GRCh38
NC_000006.11:g.157522525A>T , CM000668.1:g.157522525A>T	GRCh37
NC_000006.10:g.157564217A>T	NCBI36
NG_032093.1:g.428462A>T
NG_032093.2:g.428462A>T
NG_066624.1:g.430366A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5007A>T	ENSP00000055163.8:p.Pro1669=
ENST00000414678.8:c.5076A>T	ENSP00000412835.3:p.Pro1692=
ENST00000637015.2:c.5295A>T	ENSP00000489729.2:p.Pro1765=
ENST00000346085.10:c.5046A>T	ENSP00000344546.5:p.Pro1682=
ENST00000350026.10:c.4758A>T	ENSP00000055163.7:p.Pro1586=
ENST00000414678.7:c.3324A>T	ENSP00000412835.2:p.Pro1108=
ENST00000635849.1:c.2487A>T	ENSP00000490948.1:p.Pro829=
ENST00000635957.1:c.2118A>T	ENSP00000490385.1:p.Pro706=
ENST00000636227.1:n.3629A>T
ENST00000636254.1:n.1086A>T
ENST00000636930.2:c.5166A>T MANE Select	ENSP00000490491.2:p.Pro1722=
ENST00000636940.1:n.3163A>T
ENST00000637015.1:c.2534A>T
ENST00000637568.1:c.2448A>T
ENST00000637741.1:n.1832A>T
ENST00000637810.1:c.2508A>T	ENSP00000489636.1:p.Pro836=
ENST00000637904.1:c.2667A>T	ENSP00000490550.1:p.Pro889=
ENST00000647938.1:c.4797A>T	ENSP00000498155.1:p.Pro1599=
ENST00000346085.9:c.4797A>T	ENSP00000344546.4:p.Pro1599=
ENST00000350026.9:c.4758A>T	ENSP00000055163.7:p.Pro1586=
ENST00000414678.6:c.3324A>T	ENSP00000412835.2:p.Pro1108=
NM_017519.2:c.4758A>T	NP_059989.2:p.Pro1586=
NM_020732.3:c.4797A>T	NP_065783.3:p.Pro1599=
XM_005267069.3:c.4917A>T	XP_005267126.2:p.Pro1639=
XM_011535984.1:c.3996A>T	XP_011534286.1:p.Pro1332=
XM_011535985.1:c.3816A>T	XP_011534287.1:p.Pro1272=
XM_011535986.1:c.3576A>T	XP_011534288.1:p.Pro1192=
XM_011535987.1:c.3195A>T	XP_011534289.1:p.Pro1065=
XM_011535988.1:c.2058A>T	XP_011534290.1:p.Pro686=
NM_001346813.1:c.4917A>T	NP_001333742.1:p.Pro1639=
NM_001363725.1:c.2667A>T	NP_001350654.1:p.Pro889=
XM_011535984.2:c.5127A>T	XP_011534286.2:p.Pro1709=
XM_011535988.3:c.2058A>T	XP_011534290.1:p.Pro686=
XM_017011103.2:c.5028A>T	XP_016866592.1:p.Pro1676=
XM_017011104.1:c.4998A>T	XP_016866593.1:p.Pro1666=
XM_017011105.2:c.4968A>T	XP_016866594.1:p.Pro1656=
XM_017011106.2:c.4839A>T	XP_016866595.1:p.Pro1613=
XM_017011107.2:c.4818A>T	XP_016866596.1:p.Pro1606=
XR_002956289.1:n.5113A>T
NM_001363725.2:c.2667A>T	NP_001350654.1:p.Pro889=
NM_001371656.1:c.5046A>T	NP_001358585.1:p.Pro1682=
NM_001374820.1:c.5046A>T	NP_001361749.1:p.Pro1682=
NM_001374828.1:c.5166A>T MANE Select	NP_001361757.1:p.Pro1722=
NM_017519.3:c.5007A>T	NP_059989.3:p.Pro1669=