Canonical Allele Identifier: CA366242465

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2230572
• ClinVar RCV Id: RCV002702891
• MyVariant Identifiers: chr6:g.157522443C>G (hg19) ; chr6:g.157201309C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201309C>G , CM000668.2:g.157201309C>G	GRCh38
NC_000006.11:g.157522443C>G , CM000668.1:g.157522443C>G	GRCh37
NC_000006.10:g.157564135C>G	NCBI36
NG_032093.1:g.428380C>G
NG_032093.2:g.428380C>G
NG_066624.1:g.430284C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4925C>G	ENSP00000055163.8:p.Ser1642Cys
ENST00000414678.8:c.4994C>G	ENSP00000412835.3:p.Ser1665Cys
ENST00000637015.2:c.5213C>G	ENSP00000489729.2:p.Ser1738Cys
ENST00000346085.10:c.4964C>G	ENSP00000344546.5:p.Ser1655Cys
ENST00000350026.10:c.4676C>G	ENSP00000055163.7:p.Ser1559Cys
ENST00000414678.7:c.3242C>G	ENSP00000412835.2:p.Ser1081Cys
ENST00000635849.1:c.2405C>G	ENSP00000490948.1:p.Ser802Cys
ENST00000635957.1:c.2036C>G	ENSP00000490385.1:p.Ser679Cys
ENST00000636227.1:n.3547C>G
ENST00000636254.1:n.1004C>G
ENST00000636930.2:c.5084C>G MANE Select	ENSP00000490491.2:p.Ser1695Cys
ENST00000636940.1:n.3081C>G
ENST00000637015.1:c.2452C>G
ENST00000637568.1:c.2366C>G
ENST00000637741.1:n.1750C>G
ENST00000637810.1:c.2426C>G	ENSP00000489636.1:p.Ser809Cys
ENST00000637904.1:c.2585C>G	ENSP00000490550.1:p.Ser862Cys
ENST00000647938.1:c.4715C>G	ENSP00000498155.1:p.Ser1572Cys
ENST00000346085.9:c.4715C>G	ENSP00000344546.4:p.Ser1572Cys
ENST00000350026.9:c.4676C>G	ENSP00000055163.7:p.Ser1559Cys
ENST00000414678.6:c.3242C>G	ENSP00000412835.2:p.Ser1081Cys
NM_017519.2:c.4676C>G	NP_059989.2:p.Ser1559Cys
NM_020732.3:c.4715C>G	NP_065783.3:p.Ser1572Cys
XM_005267069.3:c.4835C>G	XP_005267126.2:p.Ser1612Cys
XM_011535984.1:c.3914C>G	XP_011534286.1:p.Ser1305Cys
XM_011535985.1:c.3734C>G	XP_011534287.1:p.Ser1245Cys
XM_011535986.1:c.3494C>G	XP_011534288.1:p.Ser1165Cys
XM_011535987.1:c.3113C>G	XP_011534289.1:p.Ser1038Cys
XM_011535988.1:c.1976C>G	XP_011534290.1:p.Ser659Cys
NM_001346813.1:c.4835C>G	NP_001333742.1:p.Ser1612Cys
NM_001363725.1:c.2585C>G	NP_001350654.1:p.Ser862Cys
XM_011535984.2:c.5045C>G	XP_011534286.2:p.Ser1682Cys
XM_011535988.3:c.1976C>G	XP_011534290.1:p.Ser659Cys
XM_017011103.2:c.4946C>G	XP_016866592.1:p.Ser1649Cys
XM_017011104.1:c.4916C>G	XP_016866593.1:p.Ser1639Cys
XM_017011105.2:c.4886C>G	XP_016866594.1:p.Ser1629Cys
XM_017011106.2:c.4757C>G	XP_016866595.1:p.Ser1586Cys
XM_017011107.2:c.4736C>G	XP_016866596.1:p.Ser1579Cys
XR_002956289.1:n.5031C>G
NM_001363725.2:c.2585C>G	NP_001350654.1:p.Ser862Cys
NM_001371656.1:c.4964C>G	NP_001358585.1:p.Ser1655Cys
NM_001374820.1:c.4964C>G	NP_001361749.1:p.Ser1655Cys
NM_001374828.1:c.5084C>G MANE Select	NP_001361757.1:p.Ser1695Cys
NM_017519.3:c.4925C>G	NP_059989.3:p.Ser1642Cys