Canonical Allele Identifier: CA366241303

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235692
• MyVariant Identifiers: chr6:g.157522089C>A (hg19) ; chr6:g.157200955C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4571C>A	ENSP00000055163.8:p.Ser1524Ter
ENST00000414678.8:c.4640C>A	ENSP00000412835.3:p.Ser1547Ter
ENST00000637015.2:c.4859C>A	ENSP00000489729.2:p.Ser1620Ter
ENST00000346085.10:c.4610C>A	ENSP00000344546.5:p.Ser1537Ter
ENST00000350026.10:c.4322C>A	ENSP00000055163.7:p.Ser1441Ter
ENST00000414678.7:c.2888C>A	ENSP00000412835.2:p.Ser963Ter
ENST00000635849.1:c.2051C>A	ENSP00000490948.1:p.Ser684Ter
ENST00000635957.1:c.1682C>A	ENSP00000490385.1:p.Ser561Ter
ENST00000636227.1:n.3193C>A
ENST00000636254.1:n.650C>A
ENST00000636930.2:c.4730C>A MANE Select	ENSP00000490491.2:p.Ser1577Ter
ENST00000636940.1:n.2727C>A
ENST00000637015.1:c.2098C>A
ENST00000637568.1:c.2012C>A
ENST00000637741.1:n.1396C>A
ENST00000637810.1:c.2072C>A	ENSP00000489636.1:p.Ser691Ter
ENST00000637904.1:c.2231C>A	ENSP00000490550.1:p.Ser744Ter
ENST00000647938.1:c.4361C>A	ENSP00000498155.1:p.Ser1454Ter
ENST00000346085.9:c.4361C>A	ENSP00000344546.4:p.Ser1454Ter
ENST00000350026.9:c.4322C>A	ENSP00000055163.7:p.Ser1441Ter
ENST00000414678.6:c.2888C>A	ENSP00000412835.2:p.Ser963Ter
NM_017519.2:c.4322C>A	NP_059989.2:p.Ser1441Ter
NM_020732.3:c.4361C>A	NP_065783.3:p.Ser1454Ter
XM_005267069.3:c.4481C>A	XP_005267126.2:p.Ser1494Ter
XM_011535984.1:c.3560C>A	XP_011534286.1:p.Ser1187Ter
XM_011535985.1:c.3380C>A	XP_011534287.1:p.Ser1127Ter
XM_011535986.1:c.3140C>A	XP_011534288.1:p.Ser1047Ter
XM_011535987.1:c.2759C>A	XP_011534289.1:p.Ser920Ter
XM_011535988.1:c.1622C>A	XP_011534290.1:p.Ser541Ter
NM_001346813.1:c.4481C>A	NP_001333742.1:p.Ser1494Ter
NM_001363725.1:c.2231C>A	NP_001350654.1:p.Ser744Ter
XM_011535984.2:c.4691C>A	XP_011534286.2:p.Ser1564Ter
XM_011535988.3:c.1622C>A	XP_011534290.1:p.Ser541Ter
XM_017011103.2:c.4592C>A	XP_016866592.1:p.Ser1531Ter
XM_017011104.1:c.4562C>A	XP_016866593.1:p.Ser1521Ter
XM_017011105.2:c.4532C>A	XP_016866594.1:p.Ser1511Ter
XM_017011106.2:c.4403C>A	XP_016866595.1:p.Ser1468Ter
XM_017011107.2:c.4382C>A	XP_016866596.1:p.Ser1461Ter
XR_002956289.1:n.4677C>A
NM_001363725.2:c.2231C>A	NP_001350654.1:p.Ser744Ter
NM_001371656.1:c.4610C>A	NP_001358585.1:p.Ser1537Ter
NM_001374820.1:c.4610C>A	NP_001361749.1:p.Ser1537Ter
NM_001374828.1:c.4730C>A MANE Select	NP_001361757.1:p.Ser1577Ter
NM_017519.3:c.4571C>A	NP_059989.3:p.Ser1524Ter