Canonical Allele Identifier: CA366239537

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366018
• gnomAD v4: 6-157198825-G-A
• MyVariant Identifiers: chr6:g.157519959G>A (hg19) ; chr6:g.157198825G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198825G>A , CM000668.2:g.157198825G>A	GRCh38
NC_000006.11:g.157519959G>A , CM000668.1:g.157519959G>A	GRCh37
NC_000006.10:g.157561651G>A	NCBI36
NG_032093.1:g.425896G>A
NG_032093.2:g.425896G>A
NG_066624.1:g.427800G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4238G>A	ENSP00000055163.8:p.Gly1413Glu
ENST00000414678.8:c.4307G>A	ENSP00000412835.3:p.Gly1436Glu
ENST00000637015.2:c.4526G>A	ENSP00000489729.2:p.Gly1509Glu
ENST00000346085.10:c.4277G>A	ENSP00000344546.5:p.Gly1426Glu
ENST00000350026.10:c.3989G>A	ENSP00000055163.7:p.Gly1330Glu
ENST00000414678.7:c.2555G>A	ENSP00000412835.2:p.Gly852Glu
ENST00000635849.1:c.1718G>A	ENSP00000490948.1:p.Gly573Glu
ENST00000635957.1:c.1349G>A	ENSP00000490385.1:p.Gly450Glu
ENST00000636227.1:n.2860G>A
ENST00000636254.1:n.317G>A
ENST00000636930.2:c.4397G>A MANE Select	ENSP00000490491.2:p.Gly1466Glu
ENST00000636940.1:n.2394G>A
ENST00000637015.1:c.1765G>A
ENST00000637568.1:c.1679G>A
ENST00000637741.1:n.1063G>A
ENST00000637810.1:c.1739G>A	ENSP00000489636.1:p.Gly580Glu
ENST00000637904.1:c.1898G>A	ENSP00000490550.1:p.Gly633Glu
ENST00000647938.1:c.4028G>A	ENSP00000498155.1:p.Gly1343Glu
ENST00000346085.9:c.4028G>A	ENSP00000344546.4:p.Gly1343Glu
ENST00000350026.9:c.3989G>A	ENSP00000055163.7:p.Gly1330Glu
ENST00000414678.6:c.2555G>A	ENSP00000412835.2:p.Gly852Glu
NM_017519.2:c.3989G>A	NP_059989.2:p.Gly1330Glu
NM_020732.3:c.4028G>A	NP_065783.3:p.Gly1343Glu
XM_005267069.3:c.4148G>A	XP_005267126.2:p.Gly1383Glu
XM_011535984.1:c.3227G>A	XP_011534286.1:p.Gly1076Glu
XM_011535985.1:c.3047G>A	XP_011534287.1:p.Gly1016Glu
XM_011535986.1:c.2807G>A	XP_011534288.1:p.Gly936Glu
XM_011535987.1:c.2426G>A	XP_011534289.1:p.Gly809Glu
XM_011535988.1:c.1289G>A	XP_011534290.1:p.Gly430Glu
NM_001346813.1:c.4148G>A	NP_001333742.1:p.Gly1383Glu
NM_001363725.1:c.1898G>A	NP_001350654.1:p.Gly633Glu
XM_011535984.2:c.4358G>A	XP_011534286.2:p.Gly1453Glu
XM_011535988.3:c.1289G>A	XP_011534290.1:p.Gly430Glu
XM_017011103.2:c.4259G>A	XP_016866592.1:p.Gly1420Glu
XM_017011104.1:c.4229G>A	XP_016866593.1:p.Gly1410Glu
XM_017011105.2:c.4199G>A	XP_016866594.1:p.Gly1400Glu
XM_017011106.2:c.4070G>A	XP_016866595.1:p.Gly1357Glu
XM_017011107.2:c.4049G>A	XP_016866596.1:p.Gly1350Glu
XR_002956289.1:n.4427-1880G>A
NM_001363725.2:c.1898G>A	NP_001350654.1:p.Gly633Glu
NM_001371656.1:c.4277G>A	NP_001358585.1:p.Gly1426Glu
NM_001374820.1:c.4277G>A	NP_001361749.1:p.Gly1426Glu
NM_001374828.1:c.4397G>A MANE Select	NP_001361757.1:p.Gly1466Glu
NM_017519.3:c.4238G>A	NP_059989.3:p.Gly1413Glu