Canonical Allele Identifier: CA4067694

Gene: ARID1B

Linked Data

• dbSNP Id: rs774071774
• ExAC: 6:157522081 G / A
• gnomAD v2: 6-157522081-G-A
• gnomAD v3: 6-157200947-G-A
• gnomAD v4: 6-157200947-G-A
• MyVariant Identifiers: chr6:g.157522081G>A (hg19) ; chr6:g.157200947G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200947G>A , CM000668.2:g.157200947G>A	GRCh38
NC_000006.11:g.157522081G>A , CM000668.1:g.157522081G>A	GRCh37
NC_000006.10:g.157563773G>A	NCBI36
NG_032093.1:g.428018G>A
NG_032093.2:g.428018G>A
NG_066624.1:g.429922G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4563G>A	ENSP00000055163.8:p.Pro1521=
ENST00000414678.8:c.4632G>A	ENSP00000412835.3:p.Pro1544=
ENST00000637015.2:c.4851G>A	ENSP00000489729.2:p.Pro1617=
ENST00000346085.10:c.4602G>A	ENSP00000344546.5:p.Pro1534=
ENST00000350026.10:c.4314G>A	ENSP00000055163.7:p.Pro1438=
ENST00000414678.7:c.2880G>A	ENSP00000412835.2:p.Pro960=
ENST00000635849.1:c.2043G>A	ENSP00000490948.1:p.Pro681=
ENST00000635957.1:c.1674G>A	ENSP00000490385.1:p.Pro558=
ENST00000636227.1:n.3185G>A
ENST00000636254.1:n.642G>A
ENST00000636930.2:c.4722G>A MANE Select	ENSP00000490491.2:p.Pro1574=
ENST00000636940.1:n.2719G>A
ENST00000637015.1:c.2090G>A
ENST00000637568.1:c.2004G>A
ENST00000637741.1:n.1388G>A
ENST00000637810.1:c.2064G>A	ENSP00000489636.1:p.Pro688=
ENST00000637904.1:c.2223G>A	ENSP00000490550.1:p.Pro741=
ENST00000647938.1:c.4353G>A	ENSP00000498155.1:p.Pro1451=
ENST00000346085.9:c.4353G>A	ENSP00000344546.4:p.Pro1451=
ENST00000350026.9:c.4314G>A	ENSP00000055163.7:p.Pro1438=
ENST00000414678.6:c.2880G>A	ENSP00000412835.2:p.Pro960=
NM_017519.2:c.4314G>A	NP_059989.2:p.Pro1438=
NM_020732.3:c.4353G>A	NP_065783.3:p.Pro1451=
XM_005267069.3:c.4473G>A	XP_005267126.2:p.Pro1491=
XM_011535984.1:c.3552G>A	XP_011534286.1:p.Pro1184=
XM_011535985.1:c.3372G>A	XP_011534287.1:p.Pro1124=
XM_011535986.1:c.3132G>A	XP_011534288.1:p.Pro1044=
XM_011535987.1:c.2751G>A	XP_011534289.1:p.Pro917=
XM_011535988.1:c.1614G>A	XP_011534290.1:p.Pro538=
NM_001346813.1:c.4473G>A	NP_001333742.1:p.Pro1491=
NM_001363725.1:c.2223G>A	NP_001350654.1:p.Pro741=
XM_011535984.2:c.4683G>A	XP_011534286.2:p.Pro1561=
XM_011535988.3:c.1614G>A	XP_011534290.1:p.Pro538=
XM_017011103.2:c.4584G>A	XP_016866592.1:p.Pro1528=
XM_017011104.1:c.4554G>A	XP_016866593.1:p.Pro1518=
XM_017011105.2:c.4524G>A	XP_016866594.1:p.Pro1508=
XM_017011106.2:c.4395G>A	XP_016866595.1:p.Pro1465=
XM_017011107.2:c.4374G>A	XP_016866596.1:p.Pro1458=
XR_002956289.1:n.4669G>A
NM_001363725.2:c.2223G>A	NP_001350654.1:p.Pro741=
NM_001371656.1:c.4602G>A	NP_001358585.1:p.Pro1534=
NM_001374820.1:c.4602G>A	NP_001361749.1:p.Pro1534=
NM_001374828.1:c.4722G>A MANE Select	NP_001361757.1:p.Pro1574=
NM_017519.3:c.4563G>A	NP_059989.3:p.Pro1521=