Canonical Allele Identifier: CA366241305

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235692
• gnomAD v3: 6-157200955-C-T
• gnomAD v4: 6-157200955-C-T
• COSMIC: COSM1236670 ; COSM1236671
• MyVariant Identifiers: chr6:g.157522089C>T (hg19) ; chr6:g.157200955C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200955C>T , CM000668.2:g.157200955C>T	GRCh38
NC_000006.11:g.157522089C>T , CM000668.1:g.157522089C>T	GRCh37
NC_000006.10:g.157563781C>T	NCBI36
NG_032093.1:g.428026C>T
NG_032093.2:g.428026C>T
NG_066624.1:g.429930C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4571C>T	ENSP00000055163.8:p.Ser1524Leu
ENST00000414678.8:c.4640C>T	ENSP00000412835.3:p.Ser1547Leu
ENST00000637015.2:c.4859C>T	ENSP00000489729.2:p.Ser1620Leu
ENST00000346085.10:c.4610C>T	ENSP00000344546.5:p.Ser1537Leu
ENST00000350026.10:c.4322C>T	ENSP00000055163.7:p.Ser1441Leu
ENST00000414678.7:c.2888C>T	ENSP00000412835.2:p.Ser963Leu
ENST00000635849.1:c.2051C>T	ENSP00000490948.1:p.Ser684Leu
ENST00000635957.1:c.1682C>T	ENSP00000490385.1:p.Ser561Leu
ENST00000636227.1:n.3193C>T
ENST00000636254.1:n.650C>T
ENST00000636930.2:c.4730C>T MANE Select	ENSP00000490491.2:p.Ser1577Leu
ENST00000636940.1:n.2727C>T
ENST00000637015.1:c.2098C>T
ENST00000637568.1:c.2012C>T
ENST00000637741.1:n.1396C>T
ENST00000637810.1:c.2072C>T	ENSP00000489636.1:p.Ser691Leu
ENST00000637904.1:c.2231C>T	ENSP00000490550.1:p.Ser744Leu
ENST00000647938.1:c.4361C>T	ENSP00000498155.1:p.Ser1454Leu
ENST00000346085.9:c.4361C>T	ENSP00000344546.4:p.Ser1454Leu
ENST00000350026.9:c.4322C>T	ENSP00000055163.7:p.Ser1441Leu
ENST00000414678.6:c.2888C>T	ENSP00000412835.2:p.Ser963Leu
NM_017519.2:c.4322C>T	NP_059989.2:p.Ser1441Leu
NM_020732.3:c.4361C>T	NP_065783.3:p.Ser1454Leu
XM_005267069.3:c.4481C>T	XP_005267126.2:p.Ser1494Leu
XM_011535984.1:c.3560C>T	XP_011534286.1:p.Ser1187Leu
XM_011535985.1:c.3380C>T	XP_011534287.1:p.Ser1127Leu
XM_011535986.1:c.3140C>T	XP_011534288.1:p.Ser1047Leu
XM_011535987.1:c.2759C>T	XP_011534289.1:p.Ser920Leu
XM_011535988.1:c.1622C>T	XP_011534290.1:p.Ser541Leu
NM_001346813.1:c.4481C>T	NP_001333742.1:p.Ser1494Leu
NM_001363725.1:c.2231C>T	NP_001350654.1:p.Ser744Leu
XM_011535984.2:c.4691C>T	XP_011534286.2:p.Ser1564Leu
XM_011535988.3:c.1622C>T	XP_011534290.1:p.Ser541Leu
XM_017011103.2:c.4592C>T	XP_016866592.1:p.Ser1531Leu
XM_017011104.1:c.4562C>T	XP_016866593.1:p.Ser1521Leu
XM_017011105.2:c.4532C>T	XP_016866594.1:p.Ser1511Leu
XM_017011106.2:c.4403C>T	XP_016866595.1:p.Ser1468Leu
XM_017011107.2:c.4382C>T	XP_016866596.1:p.Ser1461Leu
XR_002956289.1:n.4677C>T
NM_001363725.2:c.2231C>T	NP_001350654.1:p.Ser744Leu
NM_001371656.1:c.4610C>T	NP_001358585.1:p.Ser1537Leu
NM_001374820.1:c.4610C>T	NP_001361749.1:p.Ser1537Leu
NM_001374828.1:c.4730C>T MANE Select	NP_001361757.1:p.Ser1577Leu
NM_017519.3:c.4571C>T	NP_059989.3:p.Ser1524Leu