Canonical Allele Identifier: CA452784830

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522528C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201394C>T , CM000668.2:g.157201394C>T	GRCh38
NC_000006.11:g.157522528C>T , CM000668.1:g.157522528C>T	GRCh37
NC_000006.10:g.157564220C>T	NCBI36
NG_032093.1:g.428465C>T
NG_032093.2:g.428465C>T
NG_066624.1:g.430369C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5010C>T	ENSP00000055163.8:p.Pro1670=
ENST00000414678.8:c.5079C>T	ENSP00000412835.3:p.Pro1693=
ENST00000637015.2:c.5298C>T	ENSP00000489729.2:p.Pro1766=
ENST00000346085.10:c.5049C>T	ENSP00000344546.5:p.Pro1683=
ENST00000350026.10:c.4761C>T	ENSP00000055163.7:p.Pro1587=
ENST00000414678.7:c.3327C>T	ENSP00000412835.2:p.Pro1109=
ENST00000635849.1:c.2490C>T	ENSP00000490948.1:p.Pro830=
ENST00000635957.1:c.2121C>T	ENSP00000490385.1:p.Pro707=
ENST00000636227.1:n.3632C>T
ENST00000636254.1:n.1089C>T
ENST00000636930.2:c.5169C>T MANE Select	ENSP00000490491.2:p.Pro1723=
ENST00000636940.1:n.3166C>T
ENST00000637015.1:c.2537C>T
ENST00000637568.1:c.2451C>T
ENST00000637741.1:n.1835C>T
ENST00000637810.1:c.2511C>T	ENSP00000489636.1:p.Pro837=
ENST00000637904.1:c.2670C>T	ENSP00000490550.1:p.Pro890=
ENST00000647938.1:c.4800C>T	ENSP00000498155.1:p.Pro1600=
ENST00000346085.9:c.4800C>T	ENSP00000344546.4:p.Pro1600=
ENST00000350026.9:c.4761C>T	ENSP00000055163.7:p.Pro1587=
ENST00000414678.6:c.3327C>T	ENSP00000412835.2:p.Pro1109=
NM_017519.2:c.4761C>T	NP_059989.2:p.Pro1587=
NM_020732.3:c.4800C>T	NP_065783.3:p.Pro1600=
XM_005267069.3:c.4920C>T	XP_005267126.2:p.Pro1640=
XM_011535984.1:c.3999C>T	XP_011534286.1:p.Pro1333=
XM_011535985.1:c.3819C>T	XP_011534287.1:p.Pro1273=
XM_011535986.1:c.3579C>T	XP_011534288.1:p.Pro1193=
XM_011535987.1:c.3198C>T	XP_011534289.1:p.Pro1066=
XM_011535988.1:c.2061C>T	XP_011534290.1:p.Pro687=
NM_001346813.1:c.4920C>T	NP_001333742.1:p.Pro1640=
NM_001363725.1:c.2670C>T	NP_001350654.1:p.Pro890=
XM_011535984.2:c.5130C>T	XP_011534286.2:p.Pro1710=
XM_011535988.3:c.2061C>T	XP_011534290.1:p.Pro687=
XM_017011103.2:c.5031C>T	XP_016866592.1:p.Pro1677=
XM_017011104.1:c.5001C>T	XP_016866593.1:p.Pro1667=
XM_017011105.2:c.4971C>T	XP_016866594.1:p.Pro1657=
XM_017011106.2:c.4842C>T	XP_016866595.1:p.Pro1614=
XM_017011107.2:c.4821C>T	XP_016866596.1:p.Pro1607=
XR_002956289.1:n.5116C>T
NM_001363725.2:c.2670C>T	NP_001350654.1:p.Pro890=
NM_001371656.1:c.5049C>T	NP_001358585.1:p.Pro1683=
NM_001374820.1:c.5049C>T	NP_001361749.1:p.Pro1683=
NM_001374828.1:c.5169C>T MANE Select	NP_001361757.1:p.Pro1723=
NM_017519.3:c.5010C>T	NP_059989.3:p.Pro1670=