Canonical Allele Identifier: CA366388898

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1184325
• ClinVar RCV Id: RCV001542325
• dbSNP Id: rs1554226059
• MyVariant Identifiers: chr6:g.157469895G>A (hg19) ; chr6:g.157148761G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148761G>A , CM000668.2:g.157148761G>A	GRCh38
NC_000006.11:g.157469895G>A , CM000668.1:g.157469895G>A	GRCh37
NC_000006.10:g.157511587G>A	NCBI36
NG_032093.1:g.375832G>A
NG_032093.2:g.375832G>A
NG_066624.1:g.377736G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2899G>A	ENSP00000055163.8:p.Gly967Arg
ENST00000414678.8:c.2809G>A	ENSP00000412835.3:p.Gly937Arg
ENST00000637015.2:c.2899G>A	ENSP00000489729.2:p.Gly967Arg
ENST00000319584.11:c.913G>A	ENSP00000313006.7:p.Gly305Arg
ENST00000346085.10:c.2938G>A	ENSP00000344546.5:p.Gly980Arg
ENST00000350026.10:c.2650G>A	ENSP00000055163.7:p.Gly884Arg
ENST00000414678.7:c.1057G>A	ENSP00000412835.2:p.Gly353Arg
ENST00000452544.2:n.800G>A
ENST00000635849.1:c.220G>A	ENSP00000490948.1:p.Gly74Arg
ENST00000636426.1:n.33G>A
ENST00000636930.2:c.2899G>A MANE Select	ENSP00000490491.2:p.Gly967Arg
ENST00000637015.1:c.138G>A
ENST00000637810.1:c.400G>A	ENSP00000489636.1:p.Gly134Arg
ENST00000637904.1:c.400G>A	ENSP00000490550.1:p.Gly134Arg
ENST00000647938.1:c.2689G>A	ENSP00000498155.1:p.Gly897Arg
ENST00000674190.1:n.1648G>A
ENST00000319584.10:c.916G>A	ENSP00000313006.6:p.Gly306Arg
ENST00000346085.9:c.2689G>A	ENSP00000344546.4:p.Gly897Arg
ENST00000350026.9:c.2650G>A	ENSP00000055163.7:p.Gly884Arg
ENST00000414678.6:c.1057G>A	ENSP00000412835.2:p.Gly353Arg
ENST00000452544.1:n.746G>A
NM_017519.2:c.2650G>A	NP_059989.2:p.Gly884Arg
NM_020732.3:c.2689G>A	NP_065783.3:p.Gly897Arg
XM_005267069.3:c.2650G>A	XP_005267126.2:p.Gly884Arg
XM_011535984.1:c.1600G>A	XP_011534286.1:p.Gly534Arg
XM_011535985.1:c.1420G>A	XP_011534287.1:p.Gly474Arg
XM_011535986.1:c.1180G>A	XP_011534288.1:p.Gly394Arg
XM_011535987.1:c.799G>A	XP_011534289.1:p.Gly267Arg
XM_011535988.1:c.-20+15554G>A	XP_011534290.1:n.-20+15554G>A
NM_001346813.1:c.2650G>A	NP_001333742.1:p.Gly884Arg
NM_001363725.1:c.400G>A	NP_001350654.1:p.Gly134Arg
XM_011535984.2:c.2731G>A	XP_011534286.2:p.Gly911Arg
XM_011535988.3:c.-20+15554G>A	XP_011534290.1:n.-20+15554G>A
XM_017011103.2:c.2731G>A	XP_016866592.1:p.Gly911Arg
XM_017011104.1:c.2731G>A	XP_016866593.1:p.Gly911Arg
XM_017011105.2:c.2731G>A	XP_016866594.1:p.Gly911Arg
XM_017011106.2:c.2731G>A	XP_016866595.1:p.Gly911Arg
XM_017011107.2:c.2551G>A	XP_016866596.1:p.Gly851Arg
XR_002956289.1:n.2814G>A
NM_001363725.2:c.400G>A	NP_001350654.1:p.Gly134Arg
NM_001371656.1:c.2938G>A	NP_001358585.1:p.Gly980Arg
NM_001374820.1:c.2938G>A	NP_001361749.1:p.Gly980Arg
NM_001374828.1:c.2899G>A MANE Select	NP_001361757.1:p.Gly967Arg
NM_017519.3:c.2899G>A	NP_059989.3:p.Gly967Arg