Canonical Allele Identifier: CA452781589

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511184C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190050C>T , CM000668.2:g.157190050C>T	GRCh38
NC_000006.11:g.157511184C>T , CM000668.1:g.157511184C>T	GRCh37
NC_000006.10:g.157552876C>T	NCBI36
NG_032093.1:g.417121C>T
NG_032093.2:g.417121C>T
NG_066624.1:g.419025C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3912C>T	ENSP00000055163.8:p.Ile1304=
ENST00000414678.8:c.3981C>T	ENSP00000412835.3:p.Ile1327=
ENST00000637015.2:c.4200C>T	ENSP00000489729.2:p.Ile1400=
ENST00000346085.10:c.3951C>T	ENSP00000344546.5:p.Ile1317=
ENST00000350026.10:c.3663C>T	ENSP00000055163.7:p.Ile1221=
ENST00000414678.7:c.2229C>T	ENSP00000412835.2:p.Ile743=
ENST00000635849.1:c.1392C>T	ENSP00000490948.1:p.Ile464=
ENST00000635957.1:c.1023C>T	ENSP00000490385.1:p.Ile341=
ENST00000636930.2:c.4071C>T MANE Select	ENSP00000490491.2:p.Ile1357=
ENST00000636940.1:n.2068C>T
ENST00000637015.1:c.1439C>T
ENST00000637568.1:c.1353C>T
ENST00000637741.1:n.737C>T
ENST00000637810.1:c.1413C>T	ENSP00000489636.1:p.Ile471=
ENST00000637904.1:c.1572C>T	ENSP00000490550.1:p.Ile524=
ENST00000647938.1:c.3702C>T	ENSP00000498155.1:p.Ile1234=
ENST00000346085.9:c.3702C>T	ENSP00000344546.4:p.Ile1234=
ENST00000350026.9:c.3663C>T	ENSP00000055163.7:p.Ile1221=
ENST00000414678.6:c.2229C>T	ENSP00000412835.2:p.Ile743=
NM_017519.2:c.3663C>T	NP_059989.2:p.Ile1221=
NM_020732.3:c.3702C>T	NP_065783.3:p.Ile1234=
XM_005267069.3:c.3822C>T	XP_005267126.2:p.Ile1274=
XM_011535984.1:c.2901C>T	XP_011534286.1:p.Ile967=
XM_011535985.1:c.2721C>T	XP_011534287.1:p.Ile907=
XM_011535986.1:c.2481C>T	XP_011534288.1:p.Ile827=
XM_011535987.1:c.2100C>T	XP_011534289.1:p.Ile700=
XM_011535988.1:c.963C>T	XP_011534290.1:p.Ile321=
NM_001346813.1:c.3822C>T	NP_001333742.1:p.Ile1274=
NM_001363725.1:c.1572C>T	NP_001350654.1:p.Ile524=
XM_011535984.2:c.4032C>T	XP_011534286.2:p.Ile1344=
XM_011535988.3:c.963C>T	XP_011534290.1:p.Ile321=
XM_017011103.2:c.3933C>T	XP_016866592.1:p.Ile1311=
XM_017011104.1:c.3903C>T	XP_016866593.1:p.Ile1301=
XM_017011105.2:c.3873C>T	XP_016866594.1:p.Ile1291=
XM_017011106.2:c.3744C>T	XP_016866595.1:p.Ile1248=
XM_017011107.2:c.3723C>T	XP_016866596.1:p.Ile1241=
XR_002956289.1:n.4115C>T
NM_001363725.2:c.1572C>T	NP_001350654.1:p.Ile524=
NM_001371656.1:c.3951C>T	NP_001358585.1:p.Ile1317=
NM_001374820.1:c.3951C>T	NP_001361749.1:p.Ile1317=
NM_001374828.1:c.4071C>T MANE Select	NP_001361757.1:p.Ile1357=
NM_017519.3:c.3912C>T	NP_059989.3:p.Ile1304=