Canonical Allele Identifier: CA366388901

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1309718
• ClinVar RCV Id: RCV001756786
• dbSNP Id: rs2128634373
• gnomAD v4: 6-157148762-G-A
• MyVariant Identifiers: chr6:g.157469896G>A (hg19) ; chr6:g.157148762G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148762G>A , CM000668.2:g.157148762G>A	GRCh38
NC_000006.11:g.157469896G>A , CM000668.1:g.157469896G>A	GRCh37
NC_000006.10:g.157511588G>A	NCBI36
NG_032093.1:g.375833G>A
NG_032093.2:g.375833G>A
NG_066624.1:g.377737G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2900G>A	ENSP00000055163.8:p.Gly967Glu
ENST00000414678.8:c.2810G>A	ENSP00000412835.3:p.Gly937Glu
ENST00000637015.2:c.2900G>A	ENSP00000489729.2:p.Gly967Glu
ENST00000319584.11:c.914G>A	ENSP00000313006.7:p.Gly305Glu
ENST00000346085.10:c.2939G>A	ENSP00000344546.5:p.Gly980Glu
ENST00000350026.10:c.2651G>A	ENSP00000055163.7:p.Gly884Glu
ENST00000414678.7:c.1058G>A	ENSP00000412835.2:p.Gly353Glu
ENST00000452544.2:n.801G>A
ENST00000635849.1:c.221G>A	ENSP00000490948.1:p.Gly74Glu
ENST00000636426.1:n.34G>A
ENST00000636930.2:c.2900G>A MANE Select	ENSP00000490491.2:p.Gly967Glu
ENST00000637015.1:c.139G>A
ENST00000637810.1:c.401G>A	ENSP00000489636.1:p.Gly134Glu
ENST00000637904.1:c.401G>A	ENSP00000490550.1:p.Gly134Glu
ENST00000647938.1:c.2690G>A	ENSP00000498155.1:p.Gly897Glu
ENST00000674190.1:n.1649G>A
ENST00000319584.10:c.917G>A	ENSP00000313006.6:p.Gly306Glu
ENST00000346085.9:c.2690G>A	ENSP00000344546.4:p.Gly897Glu
ENST00000350026.9:c.2651G>A	ENSP00000055163.7:p.Gly884Glu
ENST00000414678.6:c.1058G>A	ENSP00000412835.2:p.Gly353Glu
ENST00000452544.1:n.747G>A
NM_017519.2:c.2651G>A	NP_059989.2:p.Gly884Glu
NM_020732.3:c.2690G>A	NP_065783.3:p.Gly897Glu
XM_005267069.3:c.2651G>A	XP_005267126.2:p.Gly884Glu
XM_011535984.1:c.1601G>A	XP_011534286.1:p.Gly534Glu
XM_011535985.1:c.1421G>A	XP_011534287.1:p.Gly474Glu
XM_011535986.1:c.1181G>A	XP_011534288.1:p.Gly394Glu
XM_011535987.1:c.800G>A	XP_011534289.1:p.Gly267Glu
XM_011535988.1:c.-20+15555G>A	XP_011534290.1:n.-20+15555G>A
NM_001346813.1:c.2651G>A	NP_001333742.1:p.Gly884Glu
NM_001363725.1:c.401G>A	NP_001350654.1:p.Gly134Glu
XM_011535984.2:c.2732G>A	XP_011534286.2:p.Gly911Glu
XM_011535988.3:c.-20+15555G>A	XP_011534290.1:n.-20+15555G>A
XM_017011103.2:c.2732G>A	XP_016866592.1:p.Gly911Glu
XM_017011104.1:c.2732G>A	XP_016866593.1:p.Gly911Glu
XM_017011105.2:c.2732G>A	XP_016866594.1:p.Gly911Glu
XM_017011106.2:c.2732G>A	XP_016866595.1:p.Gly911Glu
XM_017011107.2:c.2552G>A	XP_016866596.1:p.Gly851Glu
XR_002956289.1:n.2815G>A
NM_001363725.2:c.401G>A	NP_001350654.1:p.Gly134Glu
NM_001371656.1:c.2939G>A	NP_001358585.1:p.Gly980Glu
NM_001374820.1:c.2939G>A	NP_001361749.1:p.Gly980Glu
NM_001374828.1:c.2900G>A MANE Select	NP_001361757.1:p.Gly967Glu
NM_017519.3:c.2900G>A	NP_059989.3:p.Gly967Glu