Canonical Allele Identifier: CA452978001

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522054A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200920A>T , CM000668.2:g.157200920A>T	GRCh38
NC_000006.11:g.157522054A>T , CM000668.1:g.157522054A>T	GRCh37
NC_000006.10:g.157563746A>T	NCBI36
NG_032093.1:g.427991A>T
NG_032093.2:g.427991A>T
NG_066624.1:g.429895A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4536A>T	ENSP00000055163.8:p.Gly1512=
ENST00000414678.8:c.4605A>T	ENSP00000412835.3:p.Gly1535=
ENST00000637015.2:c.4824A>T	ENSP00000489729.2:p.Gly1608=
ENST00000346085.10:c.4575A>T	ENSP00000344546.5:p.Gly1525=
ENST00000350026.10:c.4287A>T	ENSP00000055163.7:p.Gly1429=
ENST00000414678.7:c.2853A>T	ENSP00000412835.2:p.Gly951=
ENST00000635849.1:c.2016A>T	ENSP00000490948.1:p.Gly672=
ENST00000635957.1:c.1647A>T	ENSP00000490385.1:p.Gly549=
ENST00000636227.1:n.3158A>T
ENST00000636254.1:n.615A>T
ENST00000636930.2:c.4695A>T MANE Select	ENSP00000490491.2:p.Gly1565=
ENST00000636940.1:n.2692A>T
ENST00000637015.1:c.2063A>T
ENST00000637568.1:c.1977A>T
ENST00000637741.1:n.1361A>T
ENST00000637810.1:c.2037A>T	ENSP00000489636.1:p.Gly679=
ENST00000637904.1:c.2196A>T	ENSP00000490550.1:p.Gly732=
ENST00000647938.1:c.4326A>T	ENSP00000498155.1:p.Gly1442=
ENST00000346085.9:c.4326A>T	ENSP00000344546.4:p.Gly1442=
ENST00000350026.9:c.4287A>T	ENSP00000055163.7:p.Gly1429=
ENST00000414678.6:c.2853A>T	ENSP00000412835.2:p.Gly951=
NM_017519.2:c.4287A>T	NP_059989.2:p.Gly1429=
NM_020732.3:c.4326A>T	NP_065783.3:p.Gly1442=
XM_005267069.3:c.4446A>T	XP_005267126.2:p.Gly1482=
XM_011535984.1:c.3525A>T	XP_011534286.1:p.Gly1175=
XM_011535985.1:c.3345A>T	XP_011534287.1:p.Gly1115=
XM_011535986.1:c.3105A>T	XP_011534288.1:p.Gly1035=
XM_011535987.1:c.2724A>T	XP_011534289.1:p.Gly908=
XM_011535988.1:c.1587A>T	XP_011534290.1:p.Gly529=
NM_001346813.1:c.4446A>T	NP_001333742.1:p.Gly1482=
NM_001363725.1:c.2196A>T	NP_001350654.1:p.Gly732=
XM_011535984.2:c.4656A>T	XP_011534286.2:p.Gly1552=
XM_011535988.3:c.1587A>T	XP_011534290.1:p.Gly529=
XM_017011103.2:c.4557A>T	XP_016866592.1:p.Gly1519=
XM_017011104.1:c.4527A>T	XP_016866593.1:p.Gly1509=
XM_017011105.2:c.4497A>T	XP_016866594.1:p.Gly1499=
XM_017011106.2:c.4368A>T	XP_016866595.1:p.Gly1456=
XM_017011107.2:c.4347A>T	XP_016866596.1:p.Gly1449=
XR_002956289.1:n.4642A>T
NM_001363725.2:c.2196A>T	NP_001350654.1:p.Gly732=
NM_001371656.1:c.4575A>T	NP_001358585.1:p.Gly1525=
NM_001374820.1:c.4575A>T	NP_001361749.1:p.Gly1525=
NM_001374828.1:c.4695A>T MANE Select	NP_001361757.1:p.Gly1565=
NM_017519.3:c.4536A>T	NP_059989.3:p.Gly1512=