Canonical Allele Identifier: CA366241760

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2759766
• ClinVar RCV Id: RCV003571831
• dbSNP Id: rs1306229546
• gnomAD v2: 6-157522194-C-A
• gnomAD v3: 6-157201060-C-A
• gnomAD v4: 6-157201060-C-A
• MyVariant Identifiers: chr6:g.157522194C>A (hg19) ; chr6:g.157201060C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201060C>A , CM000668.2:g.157201060C>A	GRCh38
NC_000006.11:g.157522194C>A , CM000668.1:g.157522194C>A	GRCh37
NC_000006.10:g.157563886C>A	NCBI36
NG_032093.1:g.428131C>A
NG_032093.2:g.428131C>A
NG_066624.1:g.430035C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4676C>A	ENSP00000055163.8:p.Pro1559His
ENST00000414678.8:c.4745C>A	ENSP00000412835.3:p.Pro1582His
ENST00000637015.2:c.4964C>A	ENSP00000489729.2:p.Pro1655His
ENST00000346085.10:c.4715C>A	ENSP00000344546.5:p.Pro1572His
ENST00000350026.10:c.4427C>A	ENSP00000055163.7:p.Pro1476His
ENST00000414678.7:c.2993C>A	ENSP00000412835.2:p.Pro998His
ENST00000635849.1:c.2156C>A	ENSP00000490948.1:p.Pro719His
ENST00000635957.1:c.1787C>A	ENSP00000490385.1:p.Pro596His
ENST00000636227.1:n.3298C>A
ENST00000636254.1:n.755C>A
ENST00000636930.2:c.4835C>A MANE Select	ENSP00000490491.2:p.Pro1612His
ENST00000636940.1:n.2832C>A
ENST00000637015.1:c.2203C>A
ENST00000637568.1:c.2117C>A
ENST00000637741.1:n.1501C>A
ENST00000637810.1:c.2177C>A	ENSP00000489636.1:p.Pro726His
ENST00000637904.1:c.2336C>A	ENSP00000490550.1:p.Pro779His
ENST00000647938.1:c.4466C>A	ENSP00000498155.1:p.Pro1489His
ENST00000346085.9:c.4466C>A	ENSP00000344546.4:p.Pro1489His
ENST00000350026.9:c.4427C>A	ENSP00000055163.7:p.Pro1476His
ENST00000414678.6:c.2993C>A	ENSP00000412835.2:p.Pro998His
NM_017519.2:c.4427C>A	NP_059989.2:p.Pro1476His
NM_020732.3:c.4466C>A	NP_065783.3:p.Pro1489His
XM_005267069.3:c.4586C>A	XP_005267126.2:p.Pro1529His
XM_011535984.1:c.3665C>A	XP_011534286.1:p.Pro1222His
XM_011535985.1:c.3485C>A	XP_011534287.1:p.Pro1162His
XM_011535986.1:c.3245C>A	XP_011534288.1:p.Pro1082His
XM_011535987.1:c.2864C>A	XP_011534289.1:p.Pro955His
XM_011535988.1:c.1727C>A	XP_011534290.1:p.Pro576His
NM_001346813.1:c.4586C>A	NP_001333742.1:p.Pro1529His
NM_001363725.1:c.2336C>A	NP_001350654.1:p.Pro779His
XM_011535984.2:c.4796C>A	XP_011534286.2:p.Pro1599His
XM_011535988.3:c.1727C>A	XP_011534290.1:p.Pro576His
XM_017011103.2:c.4697C>A	XP_016866592.1:p.Pro1566His
XM_017011104.1:c.4667C>A	XP_016866593.1:p.Pro1556His
XM_017011105.2:c.4637C>A	XP_016866594.1:p.Pro1546His
XM_017011106.2:c.4508C>A	XP_016866595.1:p.Pro1503His
XM_017011107.2:c.4487C>A	XP_016866596.1:p.Pro1496His
XR_002956289.1:n.4782C>A
NM_001363725.2:c.2336C>A	NP_001350654.1:p.Pro779His
NM_001371656.1:c.4715C>A	NP_001358585.1:p.Pro1572His
NM_001374820.1:c.4715C>A	NP_001361749.1:p.Pro1572His
NM_001374828.1:c.4835C>A MANE Select	NP_001361757.1:p.Pro1612His
NM_017519.3:c.4676C>A	NP_059989.3:p.Pro1559His