Canonical Allele Identifier: CA366234718

Gene: ARID1B

Linked Data

• dbSNP Id: rs1207649814
• gnomAD v2: 6-157511185-A-G
• MyVariant Identifiers: chr6:g.157511185A>G (hg19) ; chr6:g.157190051A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190051A>G , CM000668.2:g.157190051A>G	GRCh38
NC_000006.11:g.157511185A>G , CM000668.1:g.157511185A>G	GRCh37
NC_000006.10:g.157552877A>G	NCBI36
NG_032093.1:g.417122A>G
NG_032093.2:g.417122A>G
NG_066624.1:g.419026A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3913A>G	ENSP00000055163.8:p.Ser1305Gly
ENST00000414678.8:c.3982A>G	ENSP00000412835.3:p.Ser1328Gly
ENST00000637015.2:c.4201A>G	ENSP00000489729.2:p.Ser1401Gly
ENST00000346085.10:c.3952A>G	ENSP00000344546.5:p.Ser1318Gly
ENST00000350026.10:c.3664A>G	ENSP00000055163.7:p.Ser1222Gly
ENST00000414678.7:c.2230A>G	ENSP00000412835.2:p.Ser744Gly
ENST00000635849.1:c.1393A>G	ENSP00000490948.1:p.Ser465Gly
ENST00000635957.1:c.1024A>G	ENSP00000490385.1:p.Ser342Gly
ENST00000636930.2:c.4072A>G MANE Select	ENSP00000490491.2:p.Ser1358Gly
ENST00000636940.1:n.2069A>G
ENST00000637015.1:c.1440A>G
ENST00000637568.1:c.1354A>G
ENST00000637741.1:n.738A>G
ENST00000637810.1:c.1414A>G	ENSP00000489636.1:p.Ser472Gly
ENST00000637904.1:c.1573A>G	ENSP00000490550.1:p.Ser525Gly
ENST00000647938.1:c.3703A>G	ENSP00000498155.1:p.Ser1235Gly
ENST00000346085.9:c.3703A>G	ENSP00000344546.4:p.Ser1235Gly
ENST00000350026.9:c.3664A>G	ENSP00000055163.7:p.Ser1222Gly
ENST00000414678.6:c.2230A>G	ENSP00000412835.2:p.Ser744Gly
NM_017519.2:c.3664A>G	NP_059989.2:p.Ser1222Gly
NM_020732.3:c.3703A>G	NP_065783.3:p.Ser1235Gly
XM_005267069.3:c.3823A>G	XP_005267126.2:p.Ser1275Gly
XM_011535984.1:c.2902A>G	XP_011534286.1:p.Ser968Gly
XM_011535985.1:c.2722A>G	XP_011534287.1:p.Ser908Gly
XM_011535986.1:c.2482A>G	XP_011534288.1:p.Ser828Gly
XM_011535987.1:c.2101A>G	XP_011534289.1:p.Ser701Gly
XM_011535988.1:c.964A>G	XP_011534290.1:p.Ser322Gly
NM_001346813.1:c.3823A>G	NP_001333742.1:p.Ser1275Gly
NM_001363725.1:c.1573A>G	NP_001350654.1:p.Ser525Gly
XM_011535984.2:c.4033A>G	XP_011534286.2:p.Ser1345Gly
XM_011535988.3:c.964A>G	XP_011534290.1:p.Ser322Gly
XM_017011103.2:c.3934A>G	XP_016866592.1:p.Ser1312Gly
XM_017011104.1:c.3904A>G	XP_016866593.1:p.Ser1302Gly
XM_017011105.2:c.3874A>G	XP_016866594.1:p.Ser1292Gly
XM_017011106.2:c.3745A>G	XP_016866595.1:p.Ser1249Gly
XM_017011107.2:c.3724A>G	XP_016866596.1:p.Ser1242Gly
XR_002956289.1:n.4116A>G
NM_001363725.2:c.1573A>G	NP_001350654.1:p.Ser525Gly
NM_001371656.1:c.3952A>G	NP_001358585.1:p.Ser1318Gly
NM_001374820.1:c.3952A>G	NP_001361749.1:p.Ser1318Gly
NM_001374828.1:c.4072A>G MANE Select	NP_001361757.1:p.Ser1358Gly
NM_017519.3:c.3913A>G	NP_059989.3:p.Ser1305Gly