Canonical Allele Identifier: CA4067702

Gene: ARID1B

Linked Data

• dbSNP Id: rs779570779
• ExAC: 6:157522116 A / G
• gnomAD v2: 6-157522116-A-G
• gnomAD v4: 6-157200982-A-G
• MyVariant Identifiers: chr6:g.157522116A>G (hg19) ; chr6:g.157200982A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200982A>G , CM000668.2:g.157200982A>G	GRCh38
NC_000006.11:g.157522116A>G , CM000668.1:g.157522116A>G	GRCh37
NC_000006.10:g.157563808A>G	NCBI36
NG_032093.1:g.428053A>G
NG_032093.2:g.428053A>G
NG_066624.1:g.429957A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4598A>G	ENSP00000055163.8:p.Asn1533Ser
ENST00000414678.8:c.4667A>G	ENSP00000412835.3:p.Asn1556Ser
ENST00000637015.2:c.4886A>G	ENSP00000489729.2:p.Asn1629Ser
ENST00000346085.10:c.4637A>G	ENSP00000344546.5:p.Asn1546Ser
ENST00000350026.10:c.4349A>G	ENSP00000055163.7:p.Asn1450Ser
ENST00000414678.7:c.2915A>G	ENSP00000412835.2:p.Asn972Ser
ENST00000635849.1:c.2078A>G	ENSP00000490948.1:p.Asn693Ser
ENST00000635957.1:c.1709A>G	ENSP00000490385.1:p.Asn570Ser
ENST00000636227.1:n.3220A>G
ENST00000636254.1:n.677A>G
ENST00000636930.2:c.4757A>G MANE Select	ENSP00000490491.2:p.Asn1586Ser
ENST00000636940.1:n.2754A>G
ENST00000637015.1:c.2125A>G
ENST00000637568.1:c.2039A>G
ENST00000637741.1:n.1423A>G
ENST00000637810.1:c.2099A>G	ENSP00000489636.1:p.Asn700Ser
ENST00000637904.1:c.2258A>G	ENSP00000490550.1:p.Asn753Ser
ENST00000647938.1:c.4388A>G	ENSP00000498155.1:p.Asn1463Ser
ENST00000346085.9:c.4388A>G	ENSP00000344546.4:p.Asn1463Ser
ENST00000350026.9:c.4349A>G	ENSP00000055163.7:p.Asn1450Ser
ENST00000414678.6:c.2915A>G	ENSP00000412835.2:p.Asn972Ser
NM_017519.2:c.4349A>G	NP_059989.2:p.Asn1450Ser
NM_020732.3:c.4388A>G	NP_065783.3:p.Asn1463Ser
XM_005267069.3:c.4508A>G	XP_005267126.2:p.Asn1503Ser
XM_011535984.1:c.3587A>G	XP_011534286.1:p.Asn1196Ser
XM_011535985.1:c.3407A>G	XP_011534287.1:p.Asn1136Ser
XM_011535986.1:c.3167A>G	XP_011534288.1:p.Asn1056Ser
XM_011535987.1:c.2786A>G	XP_011534289.1:p.Asn929Ser
XM_011535988.1:c.1649A>G	XP_011534290.1:p.Asn550Ser
NM_001346813.1:c.4508A>G	NP_001333742.1:p.Asn1503Ser
NM_001363725.1:c.2258A>G	NP_001350654.1:p.Asn753Ser
XM_011535984.2:c.4718A>G	XP_011534286.2:p.Asn1573Ser
XM_011535988.3:c.1649A>G	XP_011534290.1:p.Asn550Ser
XM_017011103.2:c.4619A>G	XP_016866592.1:p.Asn1540Ser
XM_017011104.1:c.4589A>G	XP_016866593.1:p.Asn1530Ser
XM_017011105.2:c.4559A>G	XP_016866594.1:p.Asn1520Ser
XM_017011106.2:c.4430A>G	XP_016866595.1:p.Asn1477Ser
XM_017011107.2:c.4409A>G	XP_016866596.1:p.Asn1470Ser
XR_002956289.1:n.4704A>G
NM_001363725.2:c.2258A>G	NP_001350654.1:p.Asn753Ser
NM_001371656.1:c.4637A>G	NP_001358585.1:p.Asn1546Ser
NM_001374820.1:c.4637A>G	NP_001361749.1:p.Asn1546Ser
NM_001374828.1:c.4757A>G MANE Select	NP_001361757.1:p.Asn1586Ser
NM_017519.3:c.4598A>G	NP_059989.3:p.Asn1533Ser