Canonical Allele Identifier: CA452784752

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522495A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201361A>T , CM000668.2:g.157201361A>T	GRCh38
NC_000006.11:g.157522495A>T , CM000668.1:g.157522495A>T	GRCh37
NC_000006.10:g.157564187A>T	NCBI36
NG_032093.1:g.428432A>T
NG_032093.2:g.428432A>T
NG_066624.1:g.430336A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4977A>T	ENSP00000055163.8:p.Thr1659=
ENST00000414678.8:c.5046A>T	ENSP00000412835.3:p.Thr1682=
ENST00000637015.2:c.5265A>T	ENSP00000489729.2:p.Thr1755=
ENST00000346085.10:c.5016A>T	ENSP00000344546.5:p.Thr1672=
ENST00000350026.10:c.4728A>T	ENSP00000055163.7:p.Thr1576=
ENST00000414678.7:c.3294A>T	ENSP00000412835.2:p.Thr1098=
ENST00000635849.1:c.2457A>T	ENSP00000490948.1:p.Thr819=
ENST00000635957.1:c.2088A>T	ENSP00000490385.1:p.Thr696=
ENST00000636227.1:n.3599A>T
ENST00000636254.1:n.1056A>T
ENST00000636930.2:c.5136A>T MANE Select	ENSP00000490491.2:p.Thr1712=
ENST00000636940.1:n.3133A>T
ENST00000637015.1:c.2504A>T
ENST00000637568.1:c.2418A>T
ENST00000637741.1:n.1802A>T
ENST00000637810.1:c.2478A>T	ENSP00000489636.1:p.Thr826=
ENST00000637904.1:c.2637A>T	ENSP00000490550.1:p.Thr879=
ENST00000647938.1:c.4767A>T	ENSP00000498155.1:p.Thr1589=
ENST00000346085.9:c.4767A>T	ENSP00000344546.4:p.Thr1589=
ENST00000350026.9:c.4728A>T	ENSP00000055163.7:p.Thr1576=
ENST00000414678.6:c.3294A>T	ENSP00000412835.2:p.Thr1098=
NM_017519.2:c.4728A>T	NP_059989.2:p.Thr1576=
NM_020732.3:c.4767A>T	NP_065783.3:p.Thr1589=
XM_005267069.3:c.4887A>T	XP_005267126.2:p.Thr1629=
XM_011535984.1:c.3966A>T	XP_011534286.1:p.Thr1322=
XM_011535985.1:c.3786A>T	XP_011534287.1:p.Thr1262=
XM_011535986.1:c.3546A>T	XP_011534288.1:p.Thr1182=
XM_011535987.1:c.3165A>T	XP_011534289.1:p.Thr1055=
XM_011535988.1:c.2028A>T	XP_011534290.1:p.Thr676=
NM_001346813.1:c.4887A>T	NP_001333742.1:p.Thr1629=
NM_001363725.1:c.2637A>T	NP_001350654.1:p.Thr879=
XM_011535984.2:c.5097A>T	XP_011534286.2:p.Thr1699=
XM_011535988.3:c.2028A>T	XP_011534290.1:p.Thr676=
XM_017011103.2:c.4998A>T	XP_016866592.1:p.Thr1666=
XM_017011104.1:c.4968A>T	XP_016866593.1:p.Thr1656=
XM_017011105.2:c.4938A>T	XP_016866594.1:p.Thr1646=
XM_017011106.2:c.4809A>T	XP_016866595.1:p.Thr1603=
XM_017011107.2:c.4788A>T	XP_016866596.1:p.Thr1596=
XR_002956289.1:n.5083A>T
NM_001363725.2:c.2637A>T	NP_001350654.1:p.Thr879=
NM_001371656.1:c.5016A>T	NP_001358585.1:p.Thr1672=
NM_001374820.1:c.5016A>T	NP_001361749.1:p.Thr1672=
NM_001374828.1:c.5136A>T MANE Select	NP_001361757.1:p.Thr1712=
NM_017519.3:c.4977A>T	NP_059989.3:p.Thr1659=