Canonical Allele Identifier: CA452781889

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511247T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190113T>C , CM000668.2:g.157190113T>C	GRCh38
NC_000006.11:g.157511247T>C , CM000668.1:g.157511247T>C	GRCh37
NC_000006.10:g.157552939T>C	NCBI36
NG_032093.1:g.417184T>C
NG_032093.2:g.417184T>C
NG_066624.1:g.419088T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3975T>C	ENSP00000055163.8:p.Thr1325=
ENST00000414678.8:c.4044T>C	ENSP00000412835.3:p.Thr1348=
ENST00000637015.2:c.4263T>C	ENSP00000489729.2:p.Thr1421=
ENST00000346085.10:c.4014T>C	ENSP00000344546.5:p.Thr1338=
ENST00000350026.10:c.3726T>C	ENSP00000055163.7:p.Thr1242=
ENST00000414678.7:c.2292T>C	ENSP00000412835.2:p.Thr764=
ENST00000635849.1:c.1455T>C	ENSP00000490948.1:p.Thr485=
ENST00000635957.1:c.1086T>C	ENSP00000490385.1:p.Thr362=
ENST00000636930.2:c.4134T>C MANE Select	ENSP00000490491.2:p.Thr1378=
ENST00000636940.1:n.2131T>C
ENST00000637015.1:c.1502T>C
ENST00000637568.1:c.1416T>C
ENST00000637741.1:n.800T>C
ENST00000637810.1:c.1476T>C	ENSP00000489636.1:p.Thr492=
ENST00000637904.1:c.1635T>C	ENSP00000490550.1:p.Thr545=
ENST00000647938.1:c.3765T>C	ENSP00000498155.1:p.Thr1255=
ENST00000346085.9:c.3765T>C	ENSP00000344546.4:p.Thr1255=
ENST00000350026.9:c.3726T>C	ENSP00000055163.7:p.Thr1242=
ENST00000414678.6:c.2292T>C	ENSP00000412835.2:p.Thr764=
NM_017519.2:c.3726T>C	NP_059989.2:p.Thr1242=
NM_020732.3:c.3765T>C	NP_065783.3:p.Thr1255=
XM_005267069.3:c.3885T>C	XP_005267126.2:p.Thr1295=
XM_011535984.1:c.2964T>C	XP_011534286.1:p.Thr988=
XM_011535985.1:c.2784T>C	XP_011534287.1:p.Thr928=
XM_011535986.1:c.2544T>C	XP_011534288.1:p.Thr848=
XM_011535987.1:c.2163T>C	XP_011534289.1:p.Thr721=
XM_011535988.1:c.1026T>C	XP_011534290.1:p.Thr342=
NM_001346813.1:c.3885T>C	NP_001333742.1:p.Thr1295=
NM_001363725.1:c.1635T>C	NP_001350654.1:p.Thr545=
XM_011535984.2:c.4095T>C	XP_011534286.2:p.Thr1365=
XM_011535988.3:c.1026T>C	XP_011534290.1:p.Thr342=
XM_017011103.2:c.3996T>C	XP_016866592.1:p.Thr1332=
XM_017011104.1:c.3966T>C	XP_016866593.1:p.Thr1322=
XM_017011105.2:c.3936T>C	XP_016866594.1:p.Thr1312=
XM_017011106.2:c.3807T>C	XP_016866595.1:p.Thr1269=
XM_017011107.2:c.3786T>C	XP_016866596.1:p.Thr1262=
XR_002956289.1:n.4178T>C
NM_001363725.2:c.1635T>C	NP_001350654.1:p.Thr545=
NM_001371656.1:c.4014T>C	NP_001358585.1:p.Thr1338=
NM_001374820.1:c.4014T>C	NP_001361749.1:p.Thr1338=
NM_001374828.1:c.4134T>C MANE Select	NP_001361757.1:p.Thr1378=
NM_017519.3:c.3975T>C	NP_059989.3:p.Thr1325=