Canonical Allele Identifier: CA366241653

Gene: ARID1B

Linked Data

• dbSNP Id: rs760906582
• gnomAD v2: 6-157522173-G-A
• gnomAD v4: 6-157201039-G-A
• MyVariant Identifiers: chr6:g.157522173G>A (hg19) ; chr6:g.157201039G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201039G>A , CM000668.2:g.157201039G>A	GRCh38
NC_000006.11:g.157522173G>A , CM000668.1:g.157522173G>A	GRCh37
NC_000006.10:g.157563865G>A	NCBI36
NG_032093.1:g.428110G>A
NG_032093.2:g.428110G>A
NG_066624.1:g.430014G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4655G>A	ENSP00000055163.8:p.Gly1552Asp
ENST00000414678.8:c.4724G>A	ENSP00000412835.3:p.Gly1575Asp
ENST00000637015.2:c.4943G>A	ENSP00000489729.2:p.Gly1648Asp
ENST00000346085.10:c.4694G>A	ENSP00000344546.5:p.Gly1565Asp
ENST00000350026.10:c.4406G>A	ENSP00000055163.7:p.Gly1469Asp
ENST00000414678.7:c.2972G>A	ENSP00000412835.2:p.Gly991Asp
ENST00000635849.1:c.2135G>A	ENSP00000490948.1:p.Gly712Asp
ENST00000635957.1:c.1766G>A	ENSP00000490385.1:p.Gly589Asp
ENST00000636227.1:n.3277G>A
ENST00000636254.1:n.734G>A
ENST00000636930.2:c.4814G>A MANE Select	ENSP00000490491.2:p.Gly1605Asp
ENST00000636940.1:n.2811G>A
ENST00000637015.1:c.2182G>A
ENST00000637568.1:c.2096G>A
ENST00000637741.1:n.1480G>A
ENST00000637810.1:c.2156G>A	ENSP00000489636.1:p.Gly719Asp
ENST00000637904.1:c.2315G>A	ENSP00000490550.1:p.Gly772Asp
ENST00000647938.1:c.4445G>A	ENSP00000498155.1:p.Gly1482Asp
ENST00000346085.9:c.4445G>A	ENSP00000344546.4:p.Gly1482Asp
ENST00000350026.9:c.4406G>A	ENSP00000055163.7:p.Gly1469Asp
ENST00000414678.6:c.2972G>A	ENSP00000412835.2:p.Gly991Asp
NM_017519.2:c.4406G>A	NP_059989.2:p.Gly1469Asp
NM_020732.3:c.4445G>A	NP_065783.3:p.Gly1482Asp
XM_005267069.3:c.4565G>A	XP_005267126.2:p.Gly1522Asp
XM_011535984.1:c.3644G>A	XP_011534286.1:p.Gly1215Asp
XM_011535985.1:c.3464G>A	XP_011534287.1:p.Gly1155Asp
XM_011535986.1:c.3224G>A	XP_011534288.1:p.Gly1075Asp
XM_011535987.1:c.2843G>A	XP_011534289.1:p.Gly948Asp
XM_011535988.1:c.1706G>A	XP_011534290.1:p.Gly569Asp
NM_001346813.1:c.4565G>A	NP_001333742.1:p.Gly1522Asp
NM_001363725.1:c.2315G>A	NP_001350654.1:p.Gly772Asp
XM_011535984.2:c.4775G>A	XP_011534286.2:p.Gly1592Asp
XM_011535988.3:c.1706G>A	XP_011534290.1:p.Gly569Asp
XM_017011103.2:c.4676G>A	XP_016866592.1:p.Gly1559Asp
XM_017011104.1:c.4646G>A	XP_016866593.1:p.Gly1549Asp
XM_017011105.2:c.4616G>A	XP_016866594.1:p.Gly1539Asp
XM_017011106.2:c.4487G>A	XP_016866595.1:p.Gly1496Asp
XM_017011107.2:c.4466G>A	XP_016866596.1:p.Gly1489Asp
XR_002956289.1:n.4761G>A
NM_001363725.2:c.2315G>A	NP_001350654.1:p.Gly772Asp
NM_001371656.1:c.4694G>A	NP_001358585.1:p.Gly1565Asp
NM_001374820.1:c.4694G>A	NP_001361749.1:p.Gly1565Asp
NM_001374828.1:c.4814G>A MANE Select	NP_001361757.1:p.Gly1605Asp
NM_017519.3:c.4655G>A	NP_059989.3:p.Gly1552Asp