Canonical Allele Identifier: CA366242022

Gene: ARID1B

Linked Data

• dbSNP Id: rs1562346107
• gnomAD v4: 6-157201111-T-A
• MyVariant Identifiers: chr6:g.157522245T>A (hg19) ; chr6:g.157201111T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201111T>A , CM000668.2:g.157201111T>A	GRCh38
NC_000006.11:g.157522245T>A , CM000668.1:g.157522245T>A	GRCh37
NC_000006.10:g.157563937T>A	NCBI36
NG_032093.1:g.428182T>A
NG_032093.2:g.428182T>A
NG_066624.1:g.430086T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4727T>A	ENSP00000055163.8:p.Ile1576Lys
ENST00000414678.8:c.4796T>A	ENSP00000412835.3:p.Ile1599Lys
ENST00000637015.2:c.5015T>A	ENSP00000489729.2:p.Ile1672Lys
ENST00000346085.10:c.4766T>A	ENSP00000344546.5:p.Ile1589Lys
ENST00000350026.10:c.4478T>A	ENSP00000055163.7:p.Ile1493Lys
ENST00000414678.7:c.3044T>A	ENSP00000412835.2:p.Ile1015Lys
ENST00000635849.1:c.2207T>A	ENSP00000490948.1:p.Ile736Lys
ENST00000635957.1:c.1838T>A	ENSP00000490385.1:p.Ile613Lys
ENST00000636227.1:n.3349T>A
ENST00000636254.1:n.806T>A
ENST00000636930.2:c.4886T>A MANE Select	ENSP00000490491.2:p.Ile1629Lys
ENST00000636940.1:n.2883T>A
ENST00000637015.1:c.2254T>A
ENST00000637568.1:c.2168T>A
ENST00000637741.1:n.1552T>A
ENST00000637810.1:c.2228T>A	ENSP00000489636.1:p.Ile743Lys
ENST00000637904.1:c.2387T>A	ENSP00000490550.1:p.Ile796Lys
ENST00000647938.1:c.4517T>A	ENSP00000498155.1:p.Ile1506Lys
ENST00000346085.9:c.4517T>A	ENSP00000344546.4:p.Ile1506Lys
ENST00000350026.9:c.4478T>A	ENSP00000055163.7:p.Ile1493Lys
ENST00000414678.6:c.3044T>A	ENSP00000412835.2:p.Ile1015Lys
NM_017519.2:c.4478T>A	NP_059989.2:p.Ile1493Lys
NM_020732.3:c.4517T>A	NP_065783.3:p.Ile1506Lys
XM_005267069.3:c.4637T>A	XP_005267126.2:p.Ile1546Lys
XM_011535984.1:c.3716T>A	XP_011534286.1:p.Ile1239Lys
XM_011535985.1:c.3536T>A	XP_011534287.1:p.Ile1179Lys
XM_011535986.1:c.3296T>A	XP_011534288.1:p.Ile1099Lys
XM_011535987.1:c.2915T>A	XP_011534289.1:p.Ile972Lys
XM_011535988.1:c.1778T>A	XP_011534290.1:p.Ile593Lys
NM_001346813.1:c.4637T>A	NP_001333742.1:p.Ile1546Lys
NM_001363725.1:c.2387T>A	NP_001350654.1:p.Ile796Lys
XM_011535984.2:c.4847T>A	XP_011534286.2:p.Ile1616Lys
XM_011535988.3:c.1778T>A	XP_011534290.1:p.Ile593Lys
XM_017011103.2:c.4748T>A	XP_016866592.1:p.Ile1583Lys
XM_017011104.1:c.4718T>A	XP_016866593.1:p.Ile1573Lys
XM_017011105.2:c.4688T>A	XP_016866594.1:p.Ile1563Lys
XM_017011106.2:c.4559T>A	XP_016866595.1:p.Ile1520Lys
XM_017011107.2:c.4538T>A	XP_016866596.1:p.Ile1513Lys
XR_002956289.1:n.4833T>A
NM_001363725.2:c.2387T>A	NP_001350654.1:p.Ile796Lys
NM_001371656.1:c.4766T>A	NP_001358585.1:p.Ile1589Lys
NM_001374820.1:c.4766T>A	NP_001361749.1:p.Ile1589Lys
NM_001374828.1:c.4886T>A MANE Select	NP_001361757.1:p.Ile1629Lys
NM_017519.3:c.4727T>A	NP_059989.3:p.Ile1576Lys