Canonical Allele Identifier: CA366242537

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375921
• gnomAD v4: 6-157201324-C-G
• MyVariant Identifiers: chr6:g.157522458C>G (hg19) ; chr6:g.157201324C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201324C>G , CM000668.2:g.157201324C>G	GRCh38
NC_000006.11:g.157522458C>G , CM000668.1:g.157522458C>G	GRCh37
NC_000006.10:g.157564150C>G	NCBI36
NG_032093.1:g.428395C>G
NG_032093.2:g.428395C>G
NG_066624.1:g.430299C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4940C>G	ENSP00000055163.8:p.Ser1647Cys
ENST00000414678.8:c.5009C>G	ENSP00000412835.3:p.Ser1670Cys
ENST00000637015.2:c.5228C>G	ENSP00000489729.2:p.Ser1743Cys
ENST00000346085.10:c.4979C>G	ENSP00000344546.5:p.Ser1660Cys
ENST00000350026.10:c.4691C>G	ENSP00000055163.7:p.Ser1564Cys
ENST00000414678.7:c.3257C>G	ENSP00000412835.2:p.Ser1086Cys
ENST00000635849.1:c.2420C>G	ENSP00000490948.1:p.Ser807Cys
ENST00000635957.1:c.2051C>G	ENSP00000490385.1:p.Ser684Cys
ENST00000636227.1:n.3562C>G
ENST00000636254.1:n.1019C>G
ENST00000636930.2:c.5099C>G MANE Select	ENSP00000490491.2:p.Ser1700Cys
ENST00000636940.1:n.3096C>G
ENST00000637015.1:c.2467C>G
ENST00000637568.1:c.2381C>G
ENST00000637741.1:n.1765C>G
ENST00000637810.1:c.2441C>G	ENSP00000489636.1:p.Ser814Cys
ENST00000637904.1:c.2600C>G	ENSP00000490550.1:p.Ser867Cys
ENST00000647938.1:c.4730C>G	ENSP00000498155.1:p.Ser1577Cys
ENST00000346085.9:c.4730C>G	ENSP00000344546.4:p.Ser1577Cys
ENST00000350026.9:c.4691C>G	ENSP00000055163.7:p.Ser1564Cys
ENST00000414678.6:c.3257C>G	ENSP00000412835.2:p.Ser1086Cys
NM_017519.2:c.4691C>G	NP_059989.2:p.Ser1564Cys
NM_020732.3:c.4730C>G	NP_065783.3:p.Ser1577Cys
XM_005267069.3:c.4850C>G	XP_005267126.2:p.Ser1617Cys
XM_011535984.1:c.3929C>G	XP_011534286.1:p.Ser1310Cys
XM_011535985.1:c.3749C>G	XP_011534287.1:p.Ser1250Cys
XM_011535986.1:c.3509C>G	XP_011534288.1:p.Ser1170Cys
XM_011535987.1:c.3128C>G	XP_011534289.1:p.Ser1043Cys
XM_011535988.1:c.1991C>G	XP_011534290.1:p.Ser664Cys
NM_001346813.1:c.4850C>G	NP_001333742.1:p.Ser1617Cys
NM_001363725.1:c.2600C>G	NP_001350654.1:p.Ser867Cys
XM_011535984.2:c.5060C>G	XP_011534286.2:p.Ser1687Cys
XM_011535988.3:c.1991C>G	XP_011534290.1:p.Ser664Cys
XM_017011103.2:c.4961C>G	XP_016866592.1:p.Ser1654Cys
XM_017011104.1:c.4931C>G	XP_016866593.1:p.Ser1644Cys
XM_017011105.2:c.4901C>G	XP_016866594.1:p.Ser1634Cys
XM_017011106.2:c.4772C>G	XP_016866595.1:p.Ser1591Cys
XM_017011107.2:c.4751C>G	XP_016866596.1:p.Ser1584Cys
XR_002956289.1:n.5046C>G
NM_001363725.2:c.2600C>G	NP_001350654.1:p.Ser867Cys
NM_001371656.1:c.4979C>G	NP_001358585.1:p.Ser1660Cys
NM_001374820.1:c.4979C>G	NP_001361749.1:p.Ser1660Cys
NM_001374828.1:c.5099C>G MANE Select	NP_001361757.1:p.Ser1700Cys
NM_017519.3:c.4940C>G	NP_059989.3:p.Ser1647Cys