Canonical Allele Identifier: CA452783920

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366024
• gnomAD v4: 6-157198826-G-A
• MyVariant Identifiers: chr6:g.157519960G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198826G>A , CM000668.2:g.157198826G>A	GRCh38
NC_000006.11:g.157519960G>A , CM000668.1:g.157519960G>A	GRCh37
NC_000006.10:g.157561652G>A	NCBI36
NG_032093.1:g.425897G>A
NG_032093.2:g.425897G>A
NG_066624.1:g.427801G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4239G>A	ENSP00000055163.8:p.Gly1413=
ENST00000414678.8:c.4308G>A	ENSP00000412835.3:p.Gly1436=
ENST00000637015.2:c.4527G>A	ENSP00000489729.2:p.Gly1509=
ENST00000346085.10:c.4278G>A	ENSP00000344546.5:p.Gly1426=
ENST00000350026.10:c.3990G>A	ENSP00000055163.7:p.Gly1330=
ENST00000414678.7:c.2556G>A	ENSP00000412835.2:p.Gly852=
ENST00000635849.1:c.1719G>A	ENSP00000490948.1:p.Gly573=
ENST00000635957.1:c.1350G>A	ENSP00000490385.1:p.Gly450=
ENST00000636227.1:n.2861G>A
ENST00000636254.1:n.318G>A
ENST00000636930.2:c.4398G>A MANE Select	ENSP00000490491.2:p.Gly1466=
ENST00000636940.1:n.2395G>A
ENST00000637015.1:c.1766G>A
ENST00000637568.1:c.1680G>A
ENST00000637741.1:n.1064G>A
ENST00000637810.1:c.1740G>A	ENSP00000489636.1:p.Gly580=
ENST00000637904.1:c.1899G>A	ENSP00000490550.1:p.Gly633=
ENST00000647938.1:c.4029G>A	ENSP00000498155.1:p.Gly1343=
ENST00000346085.9:c.4029G>A	ENSP00000344546.4:p.Gly1343=
ENST00000350026.9:c.3990G>A	ENSP00000055163.7:p.Gly1330=
ENST00000414678.6:c.2556G>A	ENSP00000412835.2:p.Gly852=
NM_017519.2:c.3990G>A	NP_059989.2:p.Gly1330=
NM_020732.3:c.4029G>A	NP_065783.3:p.Gly1343=
XM_005267069.3:c.4149G>A	XP_005267126.2:p.Gly1383=
XM_011535984.1:c.3228G>A	XP_011534286.1:p.Gly1076=
XM_011535985.1:c.3048G>A	XP_011534287.1:p.Gly1016=
XM_011535986.1:c.2808G>A	XP_011534288.1:p.Gly936=
XM_011535987.1:c.2427G>A	XP_011534289.1:p.Gly809=
XM_011535988.1:c.1290G>A	XP_011534290.1:p.Gly430=
NM_001346813.1:c.4149G>A	NP_001333742.1:p.Gly1383=
NM_001363725.1:c.1899G>A	NP_001350654.1:p.Gly633=
XM_011535984.2:c.4359G>A	XP_011534286.2:p.Gly1453=
XM_011535988.3:c.1290G>A	XP_011534290.1:p.Gly430=
XM_017011103.2:c.4260G>A	XP_016866592.1:p.Gly1420=
XM_017011104.1:c.4230G>A	XP_016866593.1:p.Gly1410=
XM_017011105.2:c.4200G>A	XP_016866594.1:p.Gly1400=
XM_017011106.2:c.4071G>A	XP_016866595.1:p.Gly1357=
XM_017011107.2:c.4050G>A	XP_016866596.1:p.Gly1350=
XR_002956289.1:n.4427-1879G>A
NM_001363725.2:c.1899G>A	NP_001350654.1:p.Gly633=
NM_001371656.1:c.4278G>A	NP_001358585.1:p.Gly1426=
NM_001374820.1:c.4278G>A	NP_001361749.1:p.Gly1426=
NM_001374828.1:c.4398G>A MANE Select	NP_001361757.1:p.Gly1466=
NM_017519.3:c.4239G>A	NP_059989.3:p.Gly1413=