Canonical Allele Identifier: CA366241616

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522166G>T (hg19) ; chr6:g.157201032G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201032G>T , CM000668.2:g.157201032G>T	GRCh38
NC_000006.11:g.157522166G>T , CM000668.1:g.157522166G>T	GRCh37
NC_000006.10:g.157563858G>T	NCBI36
NG_032093.1:g.428103G>T
NG_032093.2:g.428103G>T
NG_066624.1:g.430007G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4648G>T	ENSP00000055163.8:p.Gly1550Cys
ENST00000414678.8:c.4717G>T	ENSP00000412835.3:p.Gly1573Cys
ENST00000637015.2:c.4936G>T	ENSP00000489729.2:p.Gly1646Cys
ENST00000346085.10:c.4687G>T	ENSP00000344546.5:p.Gly1563Cys
ENST00000350026.10:c.4399G>T	ENSP00000055163.7:p.Gly1467Cys
ENST00000414678.7:c.2965G>T	ENSP00000412835.2:p.Gly989Cys
ENST00000635849.1:c.2128G>T	ENSP00000490948.1:p.Gly710Cys
ENST00000635957.1:c.1759G>T	ENSP00000490385.1:p.Gly587Cys
ENST00000636227.1:n.3270G>T
ENST00000636254.1:n.727G>T
ENST00000636930.2:c.4807G>T MANE Select	ENSP00000490491.2:p.Gly1603Cys
ENST00000636940.1:n.2804G>T
ENST00000637015.1:c.2175G>T
ENST00000637568.1:c.2089G>T
ENST00000637741.1:n.1473G>T
ENST00000637810.1:c.2149G>T	ENSP00000489636.1:p.Gly717Cys
ENST00000637904.1:c.2308G>T	ENSP00000490550.1:p.Gly770Cys
ENST00000647938.1:c.4438G>T	ENSP00000498155.1:p.Gly1480Cys
ENST00000346085.9:c.4438G>T	ENSP00000344546.4:p.Gly1480Cys
ENST00000350026.9:c.4399G>T	ENSP00000055163.7:p.Gly1467Cys
ENST00000414678.6:c.2965G>T	ENSP00000412835.2:p.Gly989Cys
NM_017519.2:c.4399G>T	NP_059989.2:p.Gly1467Cys
NM_020732.3:c.4438G>T	NP_065783.3:p.Gly1480Cys
XM_005267069.3:c.4558G>T	XP_005267126.2:p.Gly1520Cys
XM_011535984.1:c.3637G>T	XP_011534286.1:p.Gly1213Cys
XM_011535985.1:c.3457G>T	XP_011534287.1:p.Gly1153Cys
XM_011535986.1:c.3217G>T	XP_011534288.1:p.Gly1073Cys
XM_011535987.1:c.2836G>T	XP_011534289.1:p.Gly946Cys
XM_011535988.1:c.1699G>T	XP_011534290.1:p.Gly567Cys
NM_001346813.1:c.4558G>T	NP_001333742.1:p.Gly1520Cys
NM_001363725.1:c.2308G>T	NP_001350654.1:p.Gly770Cys
XM_011535984.2:c.4768G>T	XP_011534286.2:p.Gly1590Cys
XM_011535988.3:c.1699G>T	XP_011534290.1:p.Gly567Cys
XM_017011103.2:c.4669G>T	XP_016866592.1:p.Gly1557Cys
XM_017011104.1:c.4639G>T	XP_016866593.1:p.Gly1547Cys
XM_017011105.2:c.4609G>T	XP_016866594.1:p.Gly1537Cys
XM_017011106.2:c.4480G>T	XP_016866595.1:p.Gly1494Cys
XM_017011107.2:c.4459G>T	XP_016866596.1:p.Gly1487Cys
XR_002956289.1:n.4754G>T
NM_001363725.2:c.2308G>T	NP_001350654.1:p.Gly770Cys
NM_001371656.1:c.4687G>T	NP_001358585.1:p.Gly1563Cys
NM_001374820.1:c.4687G>T	NP_001361749.1:p.Gly1563Cys
NM_001374828.1:c.4807G>T MANE Select	NP_001361757.1:p.Gly1603Cys
NM_017519.3:c.4648G>T	NP_059989.3:p.Gly1550Cys