Canonical Allele Identifier: CA366241845

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201075-A-G
• MyVariant Identifiers: chr6:g.157522209A>G (hg19) ; chr6:g.157201075A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201075A>G , CM000668.2:g.157201075A>G	GRCh38
NC_000006.11:g.157522209A>G , CM000668.1:g.157522209A>G	GRCh37
NC_000006.10:g.157563901A>G	NCBI36
NG_032093.1:g.428146A>G
NG_032093.2:g.428146A>G
NG_066624.1:g.430050A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4691A>G	ENSP00000055163.8:p.Asn1564Ser
ENST00000414678.8:c.4760A>G	ENSP00000412835.3:p.Asn1587Ser
ENST00000637015.2:c.4979A>G	ENSP00000489729.2:p.Asn1660Ser
ENST00000346085.10:c.4730A>G	ENSP00000344546.5:p.Asn1577Ser
ENST00000350026.10:c.4442A>G	ENSP00000055163.7:p.Asn1481Ser
ENST00000414678.7:c.3008A>G	ENSP00000412835.2:p.Asn1003Ser
ENST00000635849.1:c.2171A>G	ENSP00000490948.1:p.Asn724Ser
ENST00000635957.1:c.1802A>G	ENSP00000490385.1:p.Asn601Ser
ENST00000636227.1:n.3313A>G
ENST00000636254.1:n.770A>G
ENST00000636930.2:c.4850A>G MANE Select	ENSP00000490491.2:p.Asn1617Ser
ENST00000636940.1:n.2847A>G
ENST00000637015.1:c.2218A>G
ENST00000637568.1:c.2132A>G
ENST00000637741.1:n.1516A>G
ENST00000637810.1:c.2192A>G	ENSP00000489636.1:p.Asn731Ser
ENST00000637904.1:c.2351A>G	ENSP00000490550.1:p.Asn784Ser
ENST00000647938.1:c.4481A>G	ENSP00000498155.1:p.Asn1494Ser
ENST00000346085.9:c.4481A>G	ENSP00000344546.4:p.Asn1494Ser
ENST00000350026.9:c.4442A>G	ENSP00000055163.7:p.Asn1481Ser
ENST00000414678.6:c.3008A>G	ENSP00000412835.2:p.Asn1003Ser
NM_017519.2:c.4442A>G	NP_059989.2:p.Asn1481Ser
NM_020732.3:c.4481A>G	NP_065783.3:p.Asn1494Ser
XM_005267069.3:c.4601A>G	XP_005267126.2:p.Asn1534Ser
XM_011535984.1:c.3680A>G	XP_011534286.1:p.Asn1227Ser
XM_011535985.1:c.3500A>G	XP_011534287.1:p.Asn1167Ser
XM_011535986.1:c.3260A>G	XP_011534288.1:p.Asn1087Ser
XM_011535987.1:c.2879A>G	XP_011534289.1:p.Asn960Ser
XM_011535988.1:c.1742A>G	XP_011534290.1:p.Asn581Ser
NM_001346813.1:c.4601A>G	NP_001333742.1:p.Asn1534Ser
NM_001363725.1:c.2351A>G	NP_001350654.1:p.Asn784Ser
XM_011535984.2:c.4811A>G	XP_011534286.2:p.Asn1604Ser
XM_011535988.3:c.1742A>G	XP_011534290.1:p.Asn581Ser
XM_017011103.2:c.4712A>G	XP_016866592.1:p.Asn1571Ser
XM_017011104.1:c.4682A>G	XP_016866593.1:p.Asn1561Ser
XM_017011105.2:c.4652A>G	XP_016866594.1:p.Asn1551Ser
XM_017011106.2:c.4523A>G	XP_016866595.1:p.Asn1508Ser
XM_017011107.2:c.4502A>G	XP_016866596.1:p.Asn1501Ser
XR_002956289.1:n.4797A>G
NM_001363725.2:c.2351A>G	NP_001350654.1:p.Asn784Ser
NM_001371656.1:c.4730A>G	NP_001358585.1:p.Asn1577Ser
NM_001374820.1:c.4730A>G	NP_001361749.1:p.Asn1577Ser
NM_001374828.1:c.4850A>G MANE Select	NP_001361757.1:p.Asn1617Ser
NM_017519.3:c.4691A>G	NP_059989.3:p.Asn1564Ser