Canonical Allele Identifier: CA366242007

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4721A>C	ENSP00000055163.8:p.Gln1574Pro
ENST00000414678.8:c.4790A>C	ENSP00000412835.3:p.Gln1597Pro
ENST00000637015.2:c.5009A>C	ENSP00000489729.2:p.Gln1670Pro
ENST00000346085.10:c.4760A>C	ENSP00000344546.5:p.Gln1587Pro
ENST00000350026.10:c.4472A>C	ENSP00000055163.7:p.Gln1491Pro
ENST00000414678.7:c.3038A>C	ENSP00000412835.2:p.Gln1013Pro
ENST00000635849.1:c.2201A>C	ENSP00000490948.1:p.Gln734Pro
ENST00000635957.1:c.1832A>C	ENSP00000490385.1:p.Gln611Pro
ENST00000636227.1:n.3343A>C
ENST00000636254.1:n.800A>C
ENST00000636930.2:c.4880A>C MANE Select	ENSP00000490491.2:p.Gln1627Pro
ENST00000636940.1:n.2877A>C
ENST00000637015.1:c.2248A>C
ENST00000637568.1:c.2162A>C
ENST00000637741.1:n.1546A>C
ENST00000637810.1:c.2222A>C	ENSP00000489636.1:p.Gln741Pro
ENST00000637904.1:c.2381A>C	ENSP00000490550.1:p.Gln794Pro
ENST00000647938.1:c.4511A>C	ENSP00000498155.1:p.Gln1504Pro
ENST00000346085.9:c.4511A>C	ENSP00000344546.4:p.Gln1504Pro
ENST00000350026.9:c.4472A>C	ENSP00000055163.7:p.Gln1491Pro
ENST00000414678.6:c.3038A>C	ENSP00000412835.2:p.Gln1013Pro
NM_017519.2:c.4472A>C	NP_059989.2:p.Gln1491Pro
NM_020732.3:c.4511A>C	NP_065783.3:p.Gln1504Pro
XM_005267069.3:c.4631A>C	XP_005267126.2:p.Gln1544Pro
XM_011535984.1:c.3710A>C	XP_011534286.1:p.Gln1237Pro
XM_011535985.1:c.3530A>C	XP_011534287.1:p.Gln1177Pro
XM_011535986.1:c.3290A>C	XP_011534288.1:p.Gln1097Pro
XM_011535987.1:c.2909A>C	XP_011534289.1:p.Gln970Pro
XM_011535988.1:c.1772A>C	XP_011534290.1:p.Gln591Pro
NM_001346813.1:c.4631A>C	NP_001333742.1:p.Gln1544Pro
NM_001363725.1:c.2381A>C	NP_001350654.1:p.Gln794Pro
XM_011535984.2:c.4841A>C	XP_011534286.2:p.Gln1614Pro
XM_011535988.3:c.1772A>C	XP_011534290.1:p.Gln591Pro
XM_017011103.2:c.4742A>C	XP_016866592.1:p.Gln1581Pro
XM_017011104.1:c.4712A>C	XP_016866593.1:p.Gln1571Pro
XM_017011105.2:c.4682A>C	XP_016866594.1:p.Gln1561Pro
XM_017011106.2:c.4553A>C	XP_016866595.1:p.Gln1518Pro
XM_017011107.2:c.4532A>C	XP_016866596.1:p.Gln1511Pro
XR_002956289.1:n.4827A>C
NM_001363725.2:c.2381A>C	NP_001350654.1:p.Gln794Pro
NM_001371656.1:c.4760A>C	NP_001358585.1:p.Gln1587Pro
NM_001374820.1:c.4760A>C	NP_001361749.1:p.Gln1587Pro
NM_001374828.1:c.4880A>C MANE Select	NP_001361757.1:p.Gln1627Pro
NM_017519.3:c.4721A>C	NP_059989.3:p.Gln1574Pro