Canonical Allele Identifier: CA366241566

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201024-A-G
• MyVariant Identifiers: chr6:g.157522158A>G (hg19) ; chr6:g.157201024A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201024A>G , CM000668.2:g.157201024A>G	GRCh38
NC_000006.11:g.157522158A>G , CM000668.1:g.157522158A>G	GRCh37
NC_000006.10:g.157563850A>G	NCBI36
NG_032093.1:g.428095A>G
NG_032093.2:g.428095A>G
NG_066624.1:g.429999A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4640A>G	ENSP00000055163.8:p.Asn1547Ser
ENST00000414678.8:c.4709A>G	ENSP00000412835.3:p.Asn1570Ser
ENST00000637015.2:c.4928A>G	ENSP00000489729.2:p.Asn1643Ser
ENST00000346085.10:c.4679A>G	ENSP00000344546.5:p.Asn1560Ser
ENST00000350026.10:c.4391A>G	ENSP00000055163.7:p.Asn1464Ser
ENST00000414678.7:c.2957A>G	ENSP00000412835.2:p.Asn986Ser
ENST00000635849.1:c.2120A>G	ENSP00000490948.1:p.Asn707Ser
ENST00000635957.1:c.1751A>G	ENSP00000490385.1:p.Asn584Ser
ENST00000636227.1:n.3262A>G
ENST00000636254.1:n.719A>G
ENST00000636930.2:c.4799A>G MANE Select	ENSP00000490491.2:p.Asn1600Ser
ENST00000636940.1:n.2796A>G
ENST00000637015.1:c.2167A>G
ENST00000637568.1:c.2081A>G
ENST00000637741.1:n.1465A>G
ENST00000637810.1:c.2141A>G	ENSP00000489636.1:p.Asn714Ser
ENST00000637904.1:c.2300A>G	ENSP00000490550.1:p.Asn767Ser
ENST00000647938.1:c.4430A>G	ENSP00000498155.1:p.Asn1477Ser
ENST00000346085.9:c.4430A>G	ENSP00000344546.4:p.Asn1477Ser
ENST00000350026.9:c.4391A>G	ENSP00000055163.7:p.Asn1464Ser
ENST00000414678.6:c.2957A>G	ENSP00000412835.2:p.Asn986Ser
NM_017519.2:c.4391A>G	NP_059989.2:p.Asn1464Ser
NM_020732.3:c.4430A>G	NP_065783.3:p.Asn1477Ser
XM_005267069.3:c.4550A>G	XP_005267126.2:p.Asn1517Ser
XM_011535984.1:c.3629A>G	XP_011534286.1:p.Asn1210Ser
XM_011535985.1:c.3449A>G	XP_011534287.1:p.Asn1150Ser
XM_011535986.1:c.3209A>G	XP_011534288.1:p.Asn1070Ser
XM_011535987.1:c.2828A>G	XP_011534289.1:p.Asn943Ser
XM_011535988.1:c.1691A>G	XP_011534290.1:p.Asn564Ser
NM_001346813.1:c.4550A>G	NP_001333742.1:p.Asn1517Ser
NM_001363725.1:c.2300A>G	NP_001350654.1:p.Asn767Ser
XM_011535984.2:c.4760A>G	XP_011534286.2:p.Asn1587Ser
XM_011535988.3:c.1691A>G	XP_011534290.1:p.Asn564Ser
XM_017011103.2:c.4661A>G	XP_016866592.1:p.Asn1554Ser
XM_017011104.1:c.4631A>G	XP_016866593.1:p.Asn1544Ser
XM_017011105.2:c.4601A>G	XP_016866594.1:p.Asn1534Ser
XM_017011106.2:c.4472A>G	XP_016866595.1:p.Asn1491Ser
XM_017011107.2:c.4451A>G	XP_016866596.1:p.Asn1484Ser
XR_002956289.1:n.4746A>G
NM_001363725.2:c.2300A>G	NP_001350654.1:p.Asn767Ser
NM_001371656.1:c.4679A>G	NP_001358585.1:p.Asn1560Ser
NM_001374820.1:c.4679A>G	NP_001361749.1:p.Asn1560Ser
NM_001374828.1:c.4799A>G MANE Select	NP_001361757.1:p.Asn1600Ser
NM_017519.3:c.4640A>G	NP_059989.3:p.Asn1547Ser