Canonical Allele Identifier: CA452989854

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128463500
• MyVariant Identifiers: chr6:g.157406038A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084904A>T , CM000668.2:g.157084904A>T	GRCh38
NC_000006.11:g.157406038A>T , CM000668.1:g.157406038A>T	GRCh37
NC_000006.10:g.157447730A>T	NCBI36
NG_032093.1:g.311975A>T
NG_032093.2:g.311975A>T
NG_066624.1:g.313879A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2490A>T	ENSP00000055163.8:p.Pro830=
ENST00000414678.8:c.2490A>T	ENSP00000412835.3:p.Pro830=
ENST00000637015.2:c.2490A>T	ENSP00000489729.2:p.Pro830=
ENST00000319584.11:c.504A>T	ENSP00000313006.7:p.Pro168=
ENST00000346085.10:c.2529A>T	ENSP00000344546.5:p.Pro843=
ENST00000350026.10:c.2241A>T	ENSP00000055163.7:p.Pro747=
ENST00000414678.7:c.738A>T	ENSP00000412835.2:p.Pro246=
ENST00000452544.2:n.391A>T
ENST00000493658.2:n.139A>T
ENST00000635849.1:c.-10A>T	ENSP00000490948.1:n.-10A>T
ENST00000636930.2:c.2490A>T MANE Select	ENSP00000490491.2:p.Pro830=
ENST00000637003.1:c.-10A>T	ENSP00000489666.1:n.-10A>T
ENST00000637810.1:c.-10A>T	ENSP00000489636.1:n.-10A>T
ENST00000637904.1:c.-10A>T	ENSP00000490550.1:n.-10A>T
ENST00000647938.1:c.2280A>T	ENSP00000498155.1:p.Pro760=
ENST00000674190.1:n.1239A>T
ENST00000319584.10:c.507A>T	ENSP00000313006.6:p.Pro169=
ENST00000346085.9:c.2280A>T	ENSP00000344546.4:p.Pro760=
ENST00000350026.9:c.2241A>T	ENSP00000055163.7:p.Pro747=
ENST00000414678.6:c.738A>T	ENSP00000412835.2:p.Pro246=
ENST00000452544.1:n.349A>T
ENST00000493658.1:n.139A>T
NM_017519.2:c.2241A>T	NP_059989.2:p.Pro747=
NM_020732.3:c.2280A>T	NP_065783.3:p.Pro760=
XM_005267069.3:c.2241A>T	XP_005267126.2:p.Pro747=
XM_011535984.1:c.1191A>T	XP_011534286.1:p.Pro397=
XM_011535985.1:c.1191A>T	XP_011534287.1:p.Pro397=
XM_011535986.1:c.771A>T	XP_011534288.1:p.Pro257=
XM_011535987.1:c.390A>T	XP_011534289.1:p.Pro130=
NM_001346813.1:c.2241A>T	NP_001333742.1:p.Pro747=
NM_001363725.1:c.-10A>T	NP_001350654.1:n.-10A>T
XM_011535984.2:c.2322A>T	XP_011534286.2:p.Pro774=
XM_017011103.2:c.2322A>T	XP_016866592.1:p.Pro774=
XM_017011104.1:c.2322A>T	XP_016866593.1:p.Pro774=
XM_017011105.2:c.2322A>T	XP_016866594.1:p.Pro774=
XM_017011106.2:c.2322A>T	XP_016866595.1:p.Pro774=
XM_017011107.2:c.2322A>T	XP_016866596.1:p.Pro774=
XR_002956289.1:n.2405A>T
NM_001363725.2:c.-10A>T	NP_001350654.1:n.-10A>T
NM_001371656.1:c.2529A>T	NP_001358585.1:p.Pro843=
NM_001374820.1:c.2529A>T	NP_001361749.1:p.Pro843=
NM_001374828.1:c.2490A>T MANE Select	NP_001361757.1:p.Pro830=
NM_017519.3:c.2490A>T	NP_059989.3:p.Pro830=