Canonical Allele Identifier: CA452784798

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522516A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201382A>C , CM000668.2:g.157201382A>C	GRCh38
NC_000006.11:g.157522516A>C , CM000668.1:g.157522516A>C	GRCh37
NC_000006.10:g.157564208A>C	NCBI36
NG_032093.1:g.428453A>C
NG_032093.2:g.428453A>C
NG_066624.1:g.430357A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4998A>C	ENSP00000055163.8:p.Pro1666=
ENST00000414678.8:c.5067A>C	ENSP00000412835.3:p.Pro1689=
ENST00000637015.2:c.5286A>C	ENSP00000489729.2:p.Pro1762=
ENST00000346085.10:c.5037A>C	ENSP00000344546.5:p.Pro1679=
ENST00000350026.10:c.4749A>C	ENSP00000055163.7:p.Pro1583=
ENST00000414678.7:c.3315A>C	ENSP00000412835.2:p.Pro1105=
ENST00000635849.1:c.2478A>C	ENSP00000490948.1:p.Pro826=
ENST00000635957.1:c.2109A>C	ENSP00000490385.1:p.Pro703=
ENST00000636227.1:n.3620A>C
ENST00000636254.1:n.1077A>C
ENST00000636930.2:c.5157A>C MANE Select	ENSP00000490491.2:p.Pro1719=
ENST00000636940.1:n.3154A>C
ENST00000637015.1:c.2525A>C
ENST00000637568.1:c.2439A>C
ENST00000637741.1:n.1823A>C
ENST00000637810.1:c.2499A>C	ENSP00000489636.1:p.Pro833=
ENST00000637904.1:c.2658A>C	ENSP00000490550.1:p.Pro886=
ENST00000647938.1:c.4788A>C	ENSP00000498155.1:p.Pro1596=
ENST00000346085.9:c.4788A>C	ENSP00000344546.4:p.Pro1596=
ENST00000350026.9:c.4749A>C	ENSP00000055163.7:p.Pro1583=
ENST00000414678.6:c.3315A>C	ENSP00000412835.2:p.Pro1105=
NM_017519.2:c.4749A>C	NP_059989.2:p.Pro1583=
NM_020732.3:c.4788A>C	NP_065783.3:p.Pro1596=
XM_005267069.3:c.4908A>C	XP_005267126.2:p.Pro1636=
XM_011535984.1:c.3987A>C	XP_011534286.1:p.Pro1329=
XM_011535985.1:c.3807A>C	XP_011534287.1:p.Pro1269=
XM_011535986.1:c.3567A>C	XP_011534288.1:p.Pro1189=
XM_011535987.1:c.3186A>C	XP_011534289.1:p.Pro1062=
XM_011535988.1:c.2049A>C	XP_011534290.1:p.Pro683=
NM_001346813.1:c.4908A>C	NP_001333742.1:p.Pro1636=
NM_001363725.1:c.2658A>C	NP_001350654.1:p.Pro886=
XM_011535984.2:c.5118A>C	XP_011534286.2:p.Pro1706=
XM_011535988.3:c.2049A>C	XP_011534290.1:p.Pro683=
XM_017011103.2:c.5019A>C	XP_016866592.1:p.Pro1673=
XM_017011104.1:c.4989A>C	XP_016866593.1:p.Pro1663=
XM_017011105.2:c.4959A>C	XP_016866594.1:p.Pro1653=
XM_017011106.2:c.4830A>C	XP_016866595.1:p.Pro1610=
XM_017011107.2:c.4809A>C	XP_016866596.1:p.Pro1603=
XR_002956289.1:n.5104A>C
NM_001363725.2:c.2658A>C	NP_001350654.1:p.Pro886=
NM_001371656.1:c.5037A>C	NP_001358585.1:p.Pro1679=
NM_001374820.1:c.5037A>C	NP_001361749.1:p.Pro1679=
NM_001374828.1:c.5157A>C MANE Select	NP_001361757.1:p.Pro1719=
NM_017519.3:c.4998A>C	NP_059989.3:p.Pro1666=