Canonical Allele Identifier: CA452781599

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511205A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190071A>T , CM000668.2:g.157190071A>T	GRCh38
NC_000006.11:g.157511205A>T , CM000668.1:g.157511205A>T	GRCh37
NC_000006.10:g.157552897A>T	NCBI36
NG_032093.1:g.417142A>T
NG_032093.2:g.417142A>T
NG_066624.1:g.419046A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3933A>T	ENSP00000055163.8:p.Ser1311=
ENST00000414678.8:c.4002A>T	ENSP00000412835.3:p.Ser1334=
ENST00000637015.2:c.4221A>T	ENSP00000489729.2:p.Ser1407=
ENST00000346085.10:c.3972A>T	ENSP00000344546.5:p.Ser1324=
ENST00000350026.10:c.3684A>T	ENSP00000055163.7:p.Ser1228=
ENST00000414678.7:c.2250A>T	ENSP00000412835.2:p.Ser750=
ENST00000635849.1:c.1413A>T	ENSP00000490948.1:p.Ser471=
ENST00000635957.1:c.1044A>T	ENSP00000490385.1:p.Ser348=
ENST00000636930.2:c.4092A>T MANE Select	ENSP00000490491.2:p.Ser1364=
ENST00000636940.1:n.2089A>T
ENST00000637015.1:c.1460A>T
ENST00000637568.1:c.1374A>T
ENST00000637741.1:n.758A>T
ENST00000637810.1:c.1434A>T	ENSP00000489636.1:p.Ser478=
ENST00000637904.1:c.1593A>T	ENSP00000490550.1:p.Ser531=
ENST00000647938.1:c.3723A>T	ENSP00000498155.1:p.Ser1241=
ENST00000346085.9:c.3723A>T	ENSP00000344546.4:p.Ser1241=
ENST00000350026.9:c.3684A>T	ENSP00000055163.7:p.Ser1228=
ENST00000414678.6:c.2250A>T	ENSP00000412835.2:p.Ser750=
NM_017519.2:c.3684A>T	NP_059989.2:p.Ser1228=
NM_020732.3:c.3723A>T	NP_065783.3:p.Ser1241=
XM_005267069.3:c.3843A>T	XP_005267126.2:p.Ser1281=
XM_011535984.1:c.2922A>T	XP_011534286.1:p.Ser974=
XM_011535985.1:c.2742A>T	XP_011534287.1:p.Ser914=
XM_011535986.1:c.2502A>T	XP_011534288.1:p.Ser834=
XM_011535987.1:c.2121A>T	XP_011534289.1:p.Ser707=
XM_011535988.1:c.984A>T	XP_011534290.1:p.Ser328=
NM_001346813.1:c.3843A>T	NP_001333742.1:p.Ser1281=
NM_001363725.1:c.1593A>T	NP_001350654.1:p.Ser531=
XM_011535984.2:c.4053A>T	XP_011534286.2:p.Ser1351=
XM_011535988.3:c.984A>T	XP_011534290.1:p.Ser328=
XM_017011103.2:c.3954A>T	XP_016866592.1:p.Ser1318=
XM_017011104.1:c.3924A>T	XP_016866593.1:p.Ser1308=
XM_017011105.2:c.3894A>T	XP_016866594.1:p.Ser1298=
XM_017011106.2:c.3765A>T	XP_016866595.1:p.Ser1255=
XM_017011107.2:c.3744A>T	XP_016866596.1:p.Ser1248=
XR_002956289.1:n.4136A>T
NM_001363725.2:c.1593A>T	NP_001350654.1:p.Ser531=
NM_001371656.1:c.3972A>T	NP_001358585.1:p.Ser1324=
NM_001374820.1:c.3972A>T	NP_001361749.1:p.Ser1324=
NM_001374828.1:c.4092A>T MANE Select	NP_001361757.1:p.Ser1364=
NM_017519.3:c.3933A>T	NP_059989.3:p.Ser1311=