Canonical Allele Identifier: CA4067764

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1923866
• ClinVar RCV Id: RCV002634673
• dbSNP Id: rs746960777
• ExAC: 6:157522486 G / A
• gnomAD v2: 6-157522486-G-A
• gnomAD v3: 6-157201352-G-A
• gnomAD v4: 6-157201352-G-A
• MyVariant Identifiers: chr6:g.157522486G>A (hg19) ; chr6:g.157201352G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201352G>A , CM000668.2:g.157201352G>A	GRCh38
NC_000006.11:g.157522486G>A , CM000668.1:g.157522486G>A	GRCh37
NC_000006.10:g.157564178G>A	NCBI36
NG_032093.1:g.428423G>A
NG_032093.2:g.428423G>A
NG_066624.1:g.430327G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4968G>A	ENSP00000055163.8:p.Thr1656=
ENST00000414678.8:c.5037G>A	ENSP00000412835.3:p.Thr1679=
ENST00000637015.2:c.5256G>A	ENSP00000489729.2:p.Thr1752=
ENST00000346085.10:c.5007G>A	ENSP00000344546.5:p.Thr1669=
ENST00000350026.10:c.4719G>A	ENSP00000055163.7:p.Thr1573=
ENST00000414678.7:c.3285G>A	ENSP00000412835.2:p.Thr1095=
ENST00000635849.1:c.2448G>A	ENSP00000490948.1:p.Thr816=
ENST00000635957.1:c.2079G>A	ENSP00000490385.1:p.Thr693=
ENST00000636227.1:n.3590G>A
ENST00000636254.1:n.1047G>A
ENST00000636930.2:c.5127G>A MANE Select	ENSP00000490491.2:p.Thr1709=
ENST00000636940.1:n.3124G>A
ENST00000637015.1:c.2495G>A
ENST00000637568.1:c.2409G>A
ENST00000637741.1:n.1793G>A
ENST00000637810.1:c.2469G>A	ENSP00000489636.1:p.Thr823=
ENST00000637904.1:c.2628G>A	ENSP00000490550.1:p.Thr876=
ENST00000647938.1:c.4758G>A	ENSP00000498155.1:p.Thr1586=
ENST00000346085.9:c.4758G>A	ENSP00000344546.4:p.Thr1586=
ENST00000350026.9:c.4719G>A	ENSP00000055163.7:p.Thr1573=
ENST00000414678.6:c.3285G>A	ENSP00000412835.2:p.Thr1095=
NM_017519.2:c.4719G>A	NP_059989.2:p.Thr1573=
NM_020732.3:c.4758G>A	NP_065783.3:p.Thr1586=
XM_005267069.3:c.4878G>A	XP_005267126.2:p.Thr1626=
XM_011535984.1:c.3957G>A	XP_011534286.1:p.Thr1319=
XM_011535985.1:c.3777G>A	XP_011534287.1:p.Thr1259=
XM_011535986.1:c.3537G>A	XP_011534288.1:p.Thr1179=
XM_011535987.1:c.3156G>A	XP_011534289.1:p.Thr1052=
XM_011535988.1:c.2019G>A	XP_011534290.1:p.Thr673=
NM_001346813.1:c.4878G>A	NP_001333742.1:p.Thr1626=
NM_001363725.1:c.2628G>A	NP_001350654.1:p.Thr876=
XM_011535984.2:c.5088G>A	XP_011534286.2:p.Thr1696=
XM_011535988.3:c.2019G>A	XP_011534290.1:p.Thr673=
XM_017011103.2:c.4989G>A	XP_016866592.1:p.Thr1663=
XM_017011104.1:c.4959G>A	XP_016866593.1:p.Thr1653=
XM_017011105.2:c.4929G>A	XP_016866594.1:p.Thr1643=
XM_017011106.2:c.4800G>A	XP_016866595.1:p.Thr1600=
XM_017011107.2:c.4779G>A	XP_016866596.1:p.Thr1593=
XR_002956289.1:n.5074G>A
NM_001363725.2:c.2628G>A	NP_001350654.1:p.Thr876=
NM_001371656.1:c.5007G>A	NP_001358585.1:p.Thr1669=
NM_001374820.1:c.5007G>A	NP_001361749.1:p.Thr1669=
NM_001374828.1:c.5127G>A MANE Select	NP_001361757.1:p.Thr1709=
NM_017519.3:c.4968G>A	NP_059989.3:p.Thr1656=