Canonical Allele Identifier: CA4067746

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2781082
• ClinVar RCV Id: RCV003659784 ; RCV004539046
• dbSNP Id: rs527651886
• ExAC: 6:157522354 G / A
• gnomAD v2: 6-157522354-G-A
• gnomAD v3: 6-157201220-G-A
• gnomAD v4: 6-157201220-G-A
• COSMIC: COSM3829521 ; COSM3829522
• MyVariant Identifiers: chr6:g.157522354G>A (hg19) ; chr6:g.157201220G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201220G>A , CM000668.2:g.157201220G>A	GRCh38
NC_000006.11:g.157522354G>A , CM000668.1:g.157522354G>A	GRCh37
NC_000006.10:g.157564046G>A	NCBI36
NG_032093.1:g.428291G>A
NG_032093.2:g.428291G>A
NG_066624.1:g.430195G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4836G>A	ENSP00000055163.8:p.Thr1612=
ENST00000414678.8:c.4905G>A	ENSP00000412835.3:p.Thr1635=
ENST00000637015.2:c.5124G>A	ENSP00000489729.2:p.Thr1708=
ENST00000346085.10:c.4875G>A	ENSP00000344546.5:p.Thr1625=
ENST00000350026.10:c.4587G>A	ENSP00000055163.7:p.Thr1529=
ENST00000414678.7:c.3153G>A	ENSP00000412835.2:p.Thr1051=
ENST00000635849.1:c.2316G>A	ENSP00000490948.1:p.Thr772=
ENST00000635957.1:c.1947G>A	ENSP00000490385.1:p.Thr649=
ENST00000636227.1:n.3458G>A
ENST00000636254.1:n.915G>A
ENST00000636930.2:c.4995G>A MANE Select	ENSP00000490491.2:p.Thr1665=
ENST00000636940.1:n.2992G>A
ENST00000637015.1:c.2363G>A
ENST00000637568.1:c.2277G>A
ENST00000637741.1:n.1661G>A
ENST00000637810.1:c.2337G>A	ENSP00000489636.1:p.Thr779=
ENST00000637904.1:c.2496G>A	ENSP00000490550.1:p.Thr832=
ENST00000647938.1:c.4626G>A	ENSP00000498155.1:p.Thr1542=
ENST00000346085.9:c.4626G>A	ENSP00000344546.4:p.Thr1542=
ENST00000350026.9:c.4587G>A	ENSP00000055163.7:p.Thr1529=
ENST00000414678.6:c.3153G>A	ENSP00000412835.2:p.Thr1051=
NM_017519.2:c.4587G>A	NP_059989.2:p.Thr1529=
NM_020732.3:c.4626G>A	NP_065783.3:p.Thr1542=
XM_005267069.3:c.4746G>A	XP_005267126.2:p.Thr1582=
XM_011535984.1:c.3825G>A	XP_011534286.1:p.Thr1275=
XM_011535985.1:c.3645G>A	XP_011534287.1:p.Thr1215=
XM_011535986.1:c.3405G>A	XP_011534288.1:p.Thr1135=
XM_011535987.1:c.3024G>A	XP_011534289.1:p.Thr1008=
XM_011535988.1:c.1887G>A	XP_011534290.1:p.Thr629=
NM_001346813.1:c.4746G>A	NP_001333742.1:p.Thr1582=
NM_001363725.1:c.2496G>A	NP_001350654.1:p.Thr832=
XM_011535984.2:c.4956G>A	XP_011534286.2:p.Thr1652=
XM_011535988.3:c.1887G>A	XP_011534290.1:p.Thr629=
XM_017011103.2:c.4857G>A	XP_016866592.1:p.Thr1619=
XM_017011104.1:c.4827G>A	XP_016866593.1:p.Thr1609=
XM_017011105.2:c.4797G>A	XP_016866594.1:p.Thr1599=
XM_017011106.2:c.4668G>A	XP_016866595.1:p.Thr1556=
XM_017011107.2:c.4647G>A	XP_016866596.1:p.Thr1549=
XR_002956289.1:n.4942G>A
NM_001363725.2:c.2496G>A	NP_001350654.1:p.Thr832=
NM_001371656.1:c.4875G>A	NP_001358585.1:p.Thr1625=
NM_001374820.1:c.4875G>A	NP_001361749.1:p.Thr1625=
NM_001374828.1:c.4995G>A MANE Select	NP_001361757.1:p.Thr1665=
NM_017519.3:c.4836G>A	NP_059989.3:p.Thr1612=