Canonical Allele Identifier: CA452781513

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510816A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189682A>G , CM000668.2:g.157189682A>G	GRCh38
NC_000006.11:g.157510816A>G , CM000668.1:g.157510816A>G	GRCh37
NC_000006.10:g.157552508A>G	NCBI36
NG_032093.1:g.416753A>G
NG_032093.2:g.416753A>G
NG_066624.1:g.418657A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3801A>G	ENSP00000055163.8:p.Ser1267=
ENST00000414678.8:c.3870A>G	ENSP00000412835.3:p.Ser1290=
ENST00000637015.2:c.4089A>G	ENSP00000489729.2:p.Ser1363=
ENST00000346085.10:c.3840A>G	ENSP00000344546.5:p.Ser1280=
ENST00000350026.10:c.3552A>G	ENSP00000055163.7:p.Ser1184=
ENST00000414678.7:c.2118A>G	ENSP00000412835.2:p.Ser706=
ENST00000635849.1:c.1281A>G	ENSP00000490948.1:p.Ser427=
ENST00000635957.1:c.915A>G	ENSP00000490385.1:p.Ser305=
ENST00000636930.2:c.3960A>G MANE Select	ENSP00000490491.2:p.Ser1320=
ENST00000636940.1:n.1957A>G
ENST00000637015.1:c.1328A>G
ENST00000637568.1:c.1242A>G
ENST00000637741.1:n.626A>G
ENST00000637810.1:c.1302A>G	ENSP00000489636.1:p.Ser434=
ENST00000637904.1:c.1461A>G	ENSP00000490550.1:p.Ser487=
ENST00000647938.1:c.3591A>G	ENSP00000498155.1:p.Ser1197=
ENST00000346085.9:c.3591A>G	ENSP00000344546.4:p.Ser1197=
ENST00000350026.9:c.3552A>G	ENSP00000055163.7:p.Ser1184=
ENST00000414678.6:c.2118A>G	ENSP00000412835.2:p.Ser706=
NM_017519.2:c.3552A>G	NP_059989.2:p.Ser1184=
NM_020732.3:c.3591A>G	NP_065783.3:p.Ser1197=
XM_005267069.3:c.3711A>G	XP_005267126.2:p.Ser1237=
XM_011535984.1:c.2790A>G	XP_011534286.1:p.Ser930=
XM_011535985.1:c.2610A>G	XP_011534287.1:p.Ser870=
XM_011535986.1:c.2370A>G	XP_011534288.1:p.Ser790=
XM_011535987.1:c.1989A>G	XP_011534289.1:p.Ser663=
XM_011535988.1:c.852A>G	XP_011534290.1:p.Ser284=
NM_001346813.1:c.3711A>G	NP_001333742.1:p.Ser1237=
NM_001363725.1:c.1461A>G	NP_001350654.1:p.Ser487=
XM_011535984.2:c.3921A>G	XP_011534286.2:p.Ser1307=
XM_011535988.3:c.852A>G	XP_011534290.1:p.Ser284=
XM_017011103.2:c.3822A>G	XP_016866592.1:p.Ser1274=
XM_017011104.1:c.3792A>G	XP_016866593.1:p.Ser1264=
XM_017011105.2:c.3762A>G	XP_016866594.1:p.Ser1254=
XM_017011106.2:c.3633A>G	XP_016866595.1:p.Ser1211=
XM_017011107.2:c.3612A>G	XP_016866596.1:p.Ser1204=
XR_002956289.1:n.4004A>G
NM_001363725.2:c.1461A>G	NP_001350654.1:p.Ser487=
NM_001371656.1:c.3840A>G	NP_001358585.1:p.Ser1280=
NM_001374820.1:c.3840A>G	NP_001361749.1:p.Ser1280=
NM_001374828.1:c.3960A>G MANE Select	NP_001361757.1:p.Ser1320=
NM_017519.3:c.3801A>G	NP_059989.3:p.Ser1267=