Canonical Allele Identifier: CA366242021

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201110-A-T
• MyVariant Identifiers: chr6:g.157522244A>T (hg19) ; chr6:g.157201110A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201110A>T , CM000668.2:g.157201110A>T	GRCh38
NC_000006.11:g.157522244A>T , CM000668.1:g.157522244A>T	GRCh37
NC_000006.10:g.157563936A>T	NCBI36
NG_032093.1:g.428181A>T
NG_032093.2:g.428181A>T
NG_066624.1:g.430085A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4726A>T	ENSP00000055163.8:p.Ile1576Leu
ENST00000414678.8:c.4795A>T	ENSP00000412835.3:p.Ile1599Leu
ENST00000637015.2:c.5014A>T	ENSP00000489729.2:p.Ile1672Leu
ENST00000346085.10:c.4765A>T	ENSP00000344546.5:p.Ile1589Leu
ENST00000350026.10:c.4477A>T	ENSP00000055163.7:p.Ile1493Leu
ENST00000414678.7:c.3043A>T	ENSP00000412835.2:p.Ile1015Leu
ENST00000635849.1:c.2206A>T	ENSP00000490948.1:p.Ile736Leu
ENST00000635957.1:c.1837A>T	ENSP00000490385.1:p.Ile613Leu
ENST00000636227.1:n.3348A>T
ENST00000636254.1:n.805A>T
ENST00000636930.2:c.4885A>T MANE Select	ENSP00000490491.2:p.Ile1629Leu
ENST00000636940.1:n.2882A>T
ENST00000637015.1:c.2253A>T
ENST00000637568.1:c.2167A>T
ENST00000637741.1:n.1551A>T
ENST00000637810.1:c.2227A>T	ENSP00000489636.1:p.Ile743Leu
ENST00000637904.1:c.2386A>T	ENSP00000490550.1:p.Ile796Leu
ENST00000647938.1:c.4516A>T	ENSP00000498155.1:p.Ile1506Leu
ENST00000346085.9:c.4516A>T	ENSP00000344546.4:p.Ile1506Leu
ENST00000350026.9:c.4477A>T	ENSP00000055163.7:p.Ile1493Leu
ENST00000414678.6:c.3043A>T	ENSP00000412835.2:p.Ile1015Leu
NM_017519.2:c.4477A>T	NP_059989.2:p.Ile1493Leu
NM_020732.3:c.4516A>T	NP_065783.3:p.Ile1506Leu
XM_005267069.3:c.4636A>T	XP_005267126.2:p.Ile1546Leu
XM_011535984.1:c.3715A>T	XP_011534286.1:p.Ile1239Leu
XM_011535985.1:c.3535A>T	XP_011534287.1:p.Ile1179Leu
XM_011535986.1:c.3295A>T	XP_011534288.1:p.Ile1099Leu
XM_011535987.1:c.2914A>T	XP_011534289.1:p.Ile972Leu
XM_011535988.1:c.1777A>T	XP_011534290.1:p.Ile593Leu
NM_001346813.1:c.4636A>T	NP_001333742.1:p.Ile1546Leu
NM_001363725.1:c.2386A>T	NP_001350654.1:p.Ile796Leu
XM_011535984.2:c.4846A>T	XP_011534286.2:p.Ile1616Leu
XM_011535988.3:c.1777A>T	XP_011534290.1:p.Ile593Leu
XM_017011103.2:c.4747A>T	XP_016866592.1:p.Ile1583Leu
XM_017011104.1:c.4717A>T	XP_016866593.1:p.Ile1573Leu
XM_017011105.2:c.4687A>T	XP_016866594.1:p.Ile1563Leu
XM_017011106.2:c.4558A>T	XP_016866595.1:p.Ile1520Leu
XM_017011107.2:c.4537A>T	XP_016866596.1:p.Ile1513Leu
XR_002956289.1:n.4832A>T
NM_001363725.2:c.2386A>T	NP_001350654.1:p.Ile796Leu
NM_001371656.1:c.4765A>T	NP_001358585.1:p.Ile1589Leu
NM_001374820.1:c.4765A>T	NP_001361749.1:p.Ile1589Leu
NM_001374828.1:c.4885A>T MANE Select	NP_001361757.1:p.Ile1629Leu
NM_017519.3:c.4726A>T	NP_059989.3:p.Ile1576Leu