Canonical Allele Identifier: CA248922

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 218776
• ClinVar RCV Id: RCV000202727
• dbSNP Id: rs864309615
• COSMIC: COSM218863 ; COSM1158892
• MyVariant Identifiers: chr6:g.157502302G>A (hg19) ; chr6:g.157181168G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181168G>A , CM000668.2:g.157181168G>A	GRCh38
NC_000006.11:g.157502302G>A , CM000668.1:g.157502302G>A	GRCh37
NC_000006.10:g.157543994G>A	NCBI36
NG_032093.1:g.408239G>A
NG_032093.2:g.408239G>A
NG_066624.1:g.410143G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3545G>A	ENSP00000055163.8:p.Gly1182Asp
ENST00000414678.8:c.3614G>A	ENSP00000412835.3:p.Gly1205Asp
ENST00000637015.2:c.3833G>A	ENSP00000489729.2:p.Gly1278Asp
ENST00000319584.11:c.1718G>A	ENSP00000313006.7:p.Gly573Asp
ENST00000346085.10:c.3584G>A	ENSP00000344546.5:p.Gly1195Asp
ENST00000350026.10:c.3296G>A	ENSP00000055163.7:p.Gly1099Asp
ENST00000414678.7:c.1862G>A	ENSP00000412835.2:p.Gly621Asp
ENST00000635849.1:c.1025G>A	ENSP00000490948.1:p.Gly342Asp
ENST00000635957.1:c.659G>A	ENSP00000490385.1:p.Gly220Asp
ENST00000636930.2:c.3704G>A MANE Select	ENSP00000490491.2:p.Gly1235Asp
ENST00000636940.1:n.1701G>A
ENST00000637015.1:c.1072G>A
ENST00000637568.1:c.986G>A
ENST00000637741.1:n.370G>A
ENST00000637810.1:c.1046G>A	ENSP00000489636.1:p.Gly349Asp
ENST00000637904.1:c.1205G>A	ENSP00000490550.1:p.Gly402Asp
ENST00000647938.1:c.3335G>A	ENSP00000498155.1:p.Gly1112Asp
ENST00000319584.10:c.1721G>A	ENSP00000313006.6:p.Gly574Asp
ENST00000346085.9:c.3335G>A	ENSP00000344546.4:p.Gly1112Asp
ENST00000350026.9:c.3296G>A	ENSP00000055163.7:p.Gly1099Asp
ENST00000400790.3:c.497G>A	ENSP00000383596.3:p.Gly166Asp
ENST00000414678.6:c.1862G>A	ENSP00000412835.2:p.Gly621Asp
ENST00000478761.3:c.906G>A
NM_017519.2:c.3296G>A	NP_059989.2:p.Gly1099Asp
NM_020732.3:c.3335G>A	NP_065783.3:p.Gly1112Asp
XM_005267069.3:c.3455G>A	XP_005267126.2:p.Gly1152Asp
XM_011535984.1:c.2534G>A	XP_011534286.1:p.Gly845Asp
XM_011535985.1:c.2354G>A	XP_011534287.1:p.Gly785Asp
XM_011535986.1:c.2114G>A	XP_011534288.1:p.Gly705Asp
XM_011535987.1:c.1733G>A	XP_011534289.1:p.Gly578Asp
XM_011535988.1:c.596G>A	XP_011534290.1:p.Gly199Asp
NM_001346813.1:c.3455G>A	NP_001333742.1:p.Gly1152Asp
NM_001363725.1:c.1205G>A	NP_001350654.1:p.Gly402Asp
XM_011535984.2:c.3665G>A	XP_011534286.2:p.Gly1222Asp
XM_011535988.3:c.596G>A	XP_011534290.1:p.Gly199Asp
XM_017011103.2:c.3566G>A	XP_016866592.1:p.Gly1189Asp
XM_017011104.1:c.3536G>A	XP_016866593.1:p.Gly1179Asp
XM_017011105.2:c.3506G>A	XP_016866594.1:p.Gly1169Asp
XM_017011106.2:c.3377G>A	XP_016866595.1:p.Gly1126Asp
XM_017011107.2:c.3356G>A	XP_016866596.1:p.Gly1119Asp
XR_002956289.1:n.3748G>A
NM_001363725.2:c.1205G>A	NP_001350654.1:p.Gly402Asp
NM_001371656.1:c.3584G>A	NP_001358585.1:p.Gly1195Asp
NM_001374820.1:c.3584G>A	NP_001361749.1:p.Gly1195Asp
NM_001374828.1:c.3704G>A MANE Select	NP_001361757.1:p.Gly1235Asp
NM_017519.3:c.3545G>A	NP_059989.3:p.Gly1182Asp