Canonical Allele Identifier: CA366242361

Gene: ARID1B

Linked Data

• dbSNP Id: rs758724418
• gnomAD v3: 6-157201264-C-G
• gnomAD v4: 6-157201264-C-G
• MyVariant Identifiers: chr6:g.157522398C>G (hg19) ; chr6:g.157201264C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201264C>G , CM000668.2:g.157201264C>G	GRCh38
NC_000006.11:g.157522398C>G , CM000668.1:g.157522398C>G	GRCh37
NC_000006.10:g.157564090C>G	NCBI36
NG_032093.1:g.428335C>G
NG_032093.2:g.428335C>G
NG_066624.1:g.430239C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4880C>G	ENSP00000055163.8:p.Ala1627Gly
ENST00000414678.8:c.4949C>G	ENSP00000412835.3:p.Ala1650Gly
ENST00000637015.2:c.5168C>G	ENSP00000489729.2:p.Ala1723Gly
ENST00000346085.10:c.4919C>G	ENSP00000344546.5:p.Ala1640Gly
ENST00000350026.10:c.4631C>G	ENSP00000055163.7:p.Ala1544Gly
ENST00000414678.7:c.3197C>G	ENSP00000412835.2:p.Ala1066Gly
ENST00000635849.1:c.2360C>G	ENSP00000490948.1:p.Ala787Gly
ENST00000635957.1:c.1991C>G	ENSP00000490385.1:p.Ala664Gly
ENST00000636227.1:n.3502C>G
ENST00000636254.1:n.959C>G
ENST00000636930.2:c.5039C>G MANE Select	ENSP00000490491.2:p.Ala1680Gly
ENST00000636940.1:n.3036C>G
ENST00000637015.1:c.2407C>G
ENST00000637568.1:c.2321C>G
ENST00000637741.1:n.1705C>G
ENST00000637810.1:c.2381C>G	ENSP00000489636.1:p.Ala794Gly
ENST00000637904.1:c.2540C>G	ENSP00000490550.1:p.Ala847Gly
ENST00000647938.1:c.4670C>G	ENSP00000498155.1:p.Ala1557Gly
ENST00000346085.9:c.4670C>G	ENSP00000344546.4:p.Ala1557Gly
ENST00000350026.9:c.4631C>G	ENSP00000055163.7:p.Ala1544Gly
ENST00000414678.6:c.3197C>G	ENSP00000412835.2:p.Ala1066Gly
NM_017519.2:c.4631C>G	NP_059989.2:p.Ala1544Gly
NM_020732.3:c.4670C>G	NP_065783.3:p.Ala1557Gly
XM_005267069.3:c.4790C>G	XP_005267126.2:p.Ala1597Gly
XM_011535984.1:c.3869C>G	XP_011534286.1:p.Ala1290Gly
XM_011535985.1:c.3689C>G	XP_011534287.1:p.Ala1230Gly
XM_011535986.1:c.3449C>G	XP_011534288.1:p.Ala1150Gly
XM_011535987.1:c.3068C>G	XP_011534289.1:p.Ala1023Gly
XM_011535988.1:c.1931C>G	XP_011534290.1:p.Ala644Gly
NM_001346813.1:c.4790C>G	NP_001333742.1:p.Ala1597Gly
NM_001363725.1:c.2540C>G	NP_001350654.1:p.Ala847Gly
XM_011535984.2:c.5000C>G	XP_011534286.2:p.Ala1667Gly
XM_011535988.3:c.1931C>G	XP_011534290.1:p.Ala644Gly
XM_017011103.2:c.4901C>G	XP_016866592.1:p.Ala1634Gly
XM_017011104.1:c.4871C>G	XP_016866593.1:p.Ala1624Gly
XM_017011105.2:c.4841C>G	XP_016866594.1:p.Ala1614Gly
XM_017011106.2:c.4712C>G	XP_016866595.1:p.Ala1571Gly
XM_017011107.2:c.4691C>G	XP_016866596.1:p.Ala1564Gly
XR_002956289.1:n.4986C>G
NM_001363725.2:c.2540C>G	NP_001350654.1:p.Ala847Gly
NM_001371656.1:c.4919C>G	NP_001358585.1:p.Ala1640Gly
NM_001374820.1:c.4919C>G	NP_001361749.1:p.Ala1640Gly
NM_001374828.1:c.5039C>G MANE Select	NP_001361757.1:p.Ala1680Gly
NM_017519.3:c.4880C>G	NP_059989.3:p.Ala1627Gly