Canonical Allele Identifier: CA366242060

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522260A>T (hg19) ; chr6:g.157201126A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201126A>T , CM000668.2:g.157201126A>T	GRCh38
NC_000006.11:g.157522260A>T , CM000668.1:g.157522260A>T	GRCh37
NC_000006.10:g.157563952A>T	NCBI36
NG_032093.1:g.428197A>T
NG_032093.2:g.428197A>T
NG_066624.1:g.430101A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4742A>T	ENSP00000055163.8:p.Gln1581Leu
ENST00000414678.8:c.4811A>T	ENSP00000412835.3:p.Gln1604Leu
ENST00000637015.2:c.5030A>T	ENSP00000489729.2:p.Gln1677Leu
ENST00000346085.10:c.4781A>T	ENSP00000344546.5:p.Gln1594Leu
ENST00000350026.10:c.4493A>T	ENSP00000055163.7:p.Gln1498Leu
ENST00000414678.7:c.3059A>T	ENSP00000412835.2:p.Gln1020Leu
ENST00000635849.1:c.2222A>T	ENSP00000490948.1:p.Gln741Leu
ENST00000635957.1:c.1853A>T	ENSP00000490385.1:p.Gln618Leu
ENST00000636227.1:n.3364A>T
ENST00000636254.1:n.821A>T
ENST00000636930.2:c.4901A>T MANE Select	ENSP00000490491.2:p.Gln1634Leu
ENST00000636940.1:n.2898A>T
ENST00000637015.1:c.2269A>T
ENST00000637568.1:c.2183A>T
ENST00000637741.1:n.1567A>T
ENST00000637810.1:c.2243A>T	ENSP00000489636.1:p.Gln748Leu
ENST00000637904.1:c.2402A>T	ENSP00000490550.1:p.Gln801Leu
ENST00000647938.1:c.4532A>T	ENSP00000498155.1:p.Gln1511Leu
ENST00000346085.9:c.4532A>T	ENSP00000344546.4:p.Gln1511Leu
ENST00000350026.9:c.4493A>T	ENSP00000055163.7:p.Gln1498Leu
ENST00000414678.6:c.3059A>T	ENSP00000412835.2:p.Gln1020Leu
NM_017519.2:c.4493A>T	NP_059989.2:p.Gln1498Leu
NM_020732.3:c.4532A>T	NP_065783.3:p.Gln1511Leu
XM_005267069.3:c.4652A>T	XP_005267126.2:p.Gln1551Leu
XM_011535984.1:c.3731A>T	XP_011534286.1:p.Gln1244Leu
XM_011535985.1:c.3551A>T	XP_011534287.1:p.Gln1184Leu
XM_011535986.1:c.3311A>T	XP_011534288.1:p.Gln1104Leu
XM_011535987.1:c.2930A>T	XP_011534289.1:p.Gln977Leu
XM_011535988.1:c.1793A>T	XP_011534290.1:p.Gln598Leu
NM_001346813.1:c.4652A>T	NP_001333742.1:p.Gln1551Leu
NM_001363725.1:c.2402A>T	NP_001350654.1:p.Gln801Leu
XM_011535984.2:c.4862A>T	XP_011534286.2:p.Gln1621Leu
XM_011535988.3:c.1793A>T	XP_011534290.1:p.Gln598Leu
XM_017011103.2:c.4763A>T	XP_016866592.1:p.Gln1588Leu
XM_017011104.1:c.4733A>T	XP_016866593.1:p.Gln1578Leu
XM_017011105.2:c.4703A>T	XP_016866594.1:p.Gln1568Leu
XM_017011106.2:c.4574A>T	XP_016866595.1:p.Gln1525Leu
XM_017011107.2:c.4553A>T	XP_016866596.1:p.Gln1518Leu
XR_002956289.1:n.4848A>T
NM_001363725.2:c.2402A>T	NP_001350654.1:p.Gln801Leu
NM_001371656.1:c.4781A>T	NP_001358585.1:p.Gln1594Leu
NM_001374820.1:c.4781A>T	NP_001361749.1:p.Gln1594Leu
NM_001374828.1:c.4901A>T MANE Select	NP_001361757.1:p.Gln1634Leu
NM_017519.3:c.4742A>T	NP_059989.3:p.Gln1581Leu