Canonical Allele Identifier: CA366242009

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522239A>T (hg19) ; chr6:g.157201105A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201105A>T , CM000668.2:g.157201105A>T	GRCh38
NC_000006.11:g.157522239A>T , CM000668.1:g.157522239A>T	GRCh37
NC_000006.10:g.157563931A>T	NCBI36
NG_032093.1:g.428176A>T
NG_032093.2:g.428176A>T
NG_066624.1:g.430080A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4721A>T	ENSP00000055163.8:p.Gln1574Leu
ENST00000414678.8:c.4790A>T	ENSP00000412835.3:p.Gln1597Leu
ENST00000637015.2:c.5009A>T	ENSP00000489729.2:p.Gln1670Leu
ENST00000346085.10:c.4760A>T	ENSP00000344546.5:p.Gln1587Leu
ENST00000350026.10:c.4472A>T	ENSP00000055163.7:p.Gln1491Leu
ENST00000414678.7:c.3038A>T	ENSP00000412835.2:p.Gln1013Leu
ENST00000635849.1:c.2201A>T	ENSP00000490948.1:p.Gln734Leu
ENST00000635957.1:c.1832A>T	ENSP00000490385.1:p.Gln611Leu
ENST00000636227.1:n.3343A>T
ENST00000636254.1:n.800A>T
ENST00000636930.2:c.4880A>T MANE Select	ENSP00000490491.2:p.Gln1627Leu
ENST00000636940.1:n.2877A>T
ENST00000637015.1:c.2248A>T
ENST00000637568.1:c.2162A>T
ENST00000637741.1:n.1546A>T
ENST00000637810.1:c.2222A>T	ENSP00000489636.1:p.Gln741Leu
ENST00000637904.1:c.2381A>T	ENSP00000490550.1:p.Gln794Leu
ENST00000647938.1:c.4511A>T	ENSP00000498155.1:p.Gln1504Leu
ENST00000346085.9:c.4511A>T	ENSP00000344546.4:p.Gln1504Leu
ENST00000350026.9:c.4472A>T	ENSP00000055163.7:p.Gln1491Leu
ENST00000414678.6:c.3038A>T	ENSP00000412835.2:p.Gln1013Leu
NM_017519.2:c.4472A>T	NP_059989.2:p.Gln1491Leu
NM_020732.3:c.4511A>T	NP_065783.3:p.Gln1504Leu
XM_005267069.3:c.4631A>T	XP_005267126.2:p.Gln1544Leu
XM_011535984.1:c.3710A>T	XP_011534286.1:p.Gln1237Leu
XM_011535985.1:c.3530A>T	XP_011534287.1:p.Gln1177Leu
XM_011535986.1:c.3290A>T	XP_011534288.1:p.Gln1097Leu
XM_011535987.1:c.2909A>T	XP_011534289.1:p.Gln970Leu
XM_011535988.1:c.1772A>T	XP_011534290.1:p.Gln591Leu
NM_001346813.1:c.4631A>T	NP_001333742.1:p.Gln1544Leu
NM_001363725.1:c.2381A>T	NP_001350654.1:p.Gln794Leu
XM_011535984.2:c.4841A>T	XP_011534286.2:p.Gln1614Leu
XM_011535988.3:c.1772A>T	XP_011534290.1:p.Gln591Leu
XM_017011103.2:c.4742A>T	XP_016866592.1:p.Gln1581Leu
XM_017011104.1:c.4712A>T	XP_016866593.1:p.Gln1571Leu
XM_017011105.2:c.4682A>T	XP_016866594.1:p.Gln1561Leu
XM_017011106.2:c.4553A>T	XP_016866595.1:p.Gln1518Leu
XM_017011107.2:c.4532A>T	XP_016866596.1:p.Gln1511Leu
XR_002956289.1:n.4827A>T
NM_001363725.2:c.2381A>T	NP_001350654.1:p.Gln794Leu
NM_001371656.1:c.4760A>T	NP_001358585.1:p.Gln1587Leu
NM_001374820.1:c.4760A>T	NP_001361749.1:p.Gln1587Leu
NM_001374828.1:c.4880A>T MANE Select	NP_001361757.1:p.Gln1627Leu
NM_017519.3:c.4721A>T	NP_059989.3:p.Gln1574Leu